Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532628_532629delinsCA , CM000673.2:g.532628_532629delinsCA	GRCh38
NC_000011.9:g.532628_532629delinsCA , CM000673.1:g.532628_532629delinsCA	GRCh37
NC_000011.8:g.522628_522629delinsCA	NCBI36
NG_007666.1:g.7922_7923delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.21_22delinsTG (HRAS)	ENSP00000380722.3:n.21_22delinsTG
ENST00000417302.7:c.146_147delinsTG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.146_147delinsTG
ENST00000397594.6:c.252_253delinsTG (HRAS)	ENSP00000380722.2:n.252_253delinsTG
ENST00000417302.6:c.146_147delinsTG (HRAS)	ENSP00000388246.1:n.146_147delinsTG
ENST00000462734.2:c.187+2_187+3delinsTG (HRAS)	ENSP00000507303.1:n.187+2_187+3delinsTG
ENST00000311189.8:c.5+2_5+3delinsTG (HRAS) MANE Select	ENSP00000309845.7:n.5+2_5+3delinsTG
ENST00000311189.7:c.5+2_5+3delinsTG (HRAS)	ENSP00000309845.7:n.5+2_5+3delinsTG
ENST00000397594.5:c.146_147delinsTG (HRAS)	ENSP00000380722.1:n.146_147delinsTG
ENST00000397596.6:c.7_8delinsTG (HRAS)	ENSP00000380723.2:n.7_8delinsTG
ENST00000417302.5:c.146_147delinsTG (HRAS)	ENSP00000388246.1:n.146_147delinsTG
ENST00000451590.5:c.7_8delinsTG (HRAS)	ENSP00000407586.1:n.7_8delinsTG
ENST00000462734.1:n.350+2_350+3delinsTG (HRAS)
ENST00000478324.5:n.244_245delinsTG (HRAS)
ENST00000493230.5:c.144+2_144+3delinsTG (HRAS)	ENSP00000434023.1:n.144+2_144+3delinsTG
NM_001130442.1:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_005343.2:c.5+2_5+3delinsTG (HRAS)	NP_005334.1:n.5+2_5+3delinsTG
NM_176795.3:c.146_147delinsTG (HRAS)	NP_789765.1:n.146_147delinsTG
XM_011519875.1:c.-425+4291_-425+4292delinsCA (LRRC56)	XP_011518177.1:n.-425+4291_-425+4292delinsCA
XM_011519877.1:c.-162+4291_-162+4292delinsCA (LRRC56)	XP_011518179.1:n.-162+4291_-162+4292delinsCA
XR_242795.1:n.856+2_856+3delinsTG (HRAS)
NM_001130442.2:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_001318054.1:c.5+2_5+3delinsTG (HRAS)	NP_001304983.1:n.5+2_5+3delinsTG
NM_005343.3:c.5+2_5+3delinsTG (HRAS)	NP_005334.1:n.5+2_5+3delinsTG
NM_176795.4:c.146_147delinsTG (HRAS)	NP_789765.1:n.146_147delinsTG
XM_011519875.2:c.-425+4291_-425+4292delinsCA (LRRC56)	XP_011518177.1:n.-425+4291_-425+4292delinsCA
XM_011519877.2:c.-162+4291_-162+4292delinsCA (LRRC56)	XP_011518179.1:n.-162+4291_-162+4292delinsCA
XM_017017167.1:c.-500+4291_-500+4292delinsCA (LRRC56)	XP_016872656.1:n.-500+4291_-500+4292delinsCA
XM_017017168.1:c.-500+4291_-500+4292delinsCA (LRRC56)	XP_016872657.1:n.-500+4291_-500+4292delinsCA
NM_005343.4:c.5+2_5+3delinsTG (HRAS) MANE Select	NP_005334.1:n.5+2_5+3delinsTG
NM_001318054.2:c.5+2_5+3delinsTG (HRAS)	NP_001304983.1:n.5+2_5+3delinsTG
NM_001130442.3:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_176795.5:c.146_147delinsTG (HRAS) MANE Plus Clinical	NP_789765.1:n.146_147delinsTG

HGVS	Amino-acid Change
ENST00000397594.7:c.21_22delinsTG (HRAS)	ENSP00000380722.3:n.21_22delinsTG
ENST00000417302.7:c.146_147delinsTG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.146_147delinsTG
ENST00000397594.6:c.252_253delinsTG (HRAS)	ENSP00000380722.2:n.252_253delinsTG
ENST00000417302.6:c.146_147delinsTG (HRAS)	ENSP00000388246.1:n.146_147delinsTG
ENST00000462734.2:c.187+2_187+3delinsTG (HRAS)	ENSP00000507303.1:n.187+2_187+3delinsTG
ENST00000311189.8:c.5+2_5+3delinsTG (HRAS) MANE Select	ENSP00000309845.7:n.5+2_5+3delinsTG
ENST00000311189.7:c.5+2_5+3delinsTG (HRAS)	ENSP00000309845.7:n.5+2_5+3delinsTG
ENST00000397594.5:c.146_147delinsTG (HRAS)	ENSP00000380722.1:n.146_147delinsTG
ENST00000397596.6:c.7_8delinsTG (HRAS)	ENSP00000380723.2:n.7_8delinsTG
ENST00000417302.5:c.146_147delinsTG (HRAS)	ENSP00000388246.1:n.146_147delinsTG
ENST00000451590.5:c.7_8delinsTG (HRAS)	ENSP00000407586.1:n.7_8delinsTG
ENST00000462734.1:n.350+2_350+3delinsTG (HRAS)
ENST00000478324.5:n.244_245delinsTG (HRAS)
ENST00000493230.5:c.144+2_144+3delinsTG (HRAS)	ENSP00000434023.1:n.144+2_144+3delinsTG
NM_001130442.1:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_005343.2:c.5+2_5+3delinsTG (HRAS)	NP_005334.1:n.5+2_5+3delinsTG
NM_176795.3:c.146_147delinsTG (HRAS)	NP_789765.1:n.146_147delinsTG
XM_011519875.1:c.-425+4291_-425+4292delinsCA (LRRC56)	XP_011518177.1:n.-425+4291_-425+4292delinsCA
XM_011519877.1:c.-162+4291_-162+4292delinsCA (LRRC56)	XP_011518179.1:n.-162+4291_-162+4292delinsCA
XR_242795.1:n.856+2_856+3delinsTG (HRAS)
NM_001130442.2:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_001318054.1:c.5+2_5+3delinsTG (HRAS)	NP_001304983.1:n.5+2_5+3delinsTG
NM_005343.3:c.5+2_5+3delinsTG (HRAS)	NP_005334.1:n.5+2_5+3delinsTG
NM_176795.4:c.146_147delinsTG (HRAS)	NP_789765.1:n.146_147delinsTG
XM_011519875.2:c.-425+4291_-425+4292delinsCA (LRRC56)	XP_011518177.1:n.-425+4291_-425+4292delinsCA
XM_011519877.2:c.-162+4291_-162+4292delinsCA (LRRC56)	XP_011518179.1:n.-162+4291_-162+4292delinsCA
XM_017017167.1:c.-500+4291_-500+4292delinsCA (LRRC56)	XP_016872656.1:n.-500+4291_-500+4292delinsCA
XM_017017168.1:c.-500+4291_-500+4292delinsCA (LRRC56)	XP_016872657.1:n.-500+4291_-500+4292delinsCA
NM_005343.4:c.5+2_5+3delinsTG (HRAS) MANE Select	NP_005334.1:n.5+2_5+3delinsTG
NM_001318054.2:c.5+2_5+3delinsTG (HRAS)	NP_001304983.1:n.5+2_5+3delinsTG
NM_001130442.3:c.7_8delinsTG (HRAS)	NP_001123914.1:n.7_8delinsTG
NM_176795.5:c.146_147delinsTG (HRAS) MANE Plus Clinical	NP_789765.1:n.146_147delinsTG