Canonical Allele Identifier: CA653923712

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532455_532456insT , CM000673.2:g.532455_532456insT GRCh38
NC_000011.9:g.532455_532456insT , CM000673.1:g.532455_532456insT GRCh37
NC_000011.8:g.522455_522456insT NCBI36
NG_007666.1:g.8095_8096insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*194_*195insA (HRAS) ENSP00000380722.3:n.*194_*195insA
ENST00000417302.7:c.*319_*320insA (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*319_*320insA
ENST00000397594.6:c.425_426insA (HRAS) ENSP00000380722.2:n.425_426insA
ENST00000417302.6:c.*319_*320insA (HRAS) ENSP00000388246.1:n.*319_*320insA
ENST00000462734.2:c.*254_*255insA (HRAS) ENSP00000507303.1:n.*254_*255insA
ENST00000311189.8:c.*72_*73insA (HRAS) MANE Select ENSP00000309845.7:n.*72_*73insA
ENST00000311189.7:c.*72_*73insA (HRAS) ENSP00000309845.7:n.*72_*73insA
ENST00000397594.5:c.*319_*320insA (HRAS) ENSP00000380722.1:n.*319_*320insA
ENST00000397596.6:c.*180_*181insA (HRAS) ENSP00000380723.2:n.*180_*181insA
ENST00000417302.5:c.*319_*320insA (HRAS) ENSP00000388246.1:n.*319_*320insA
ENST00000451590.5:c.*180_*181insA (HRAS) ENSP00000407586.1:n.*180_*181insA
ENST00000462734.1:n.417_418insA (HRAS)
ENST00000478324.5:n.417_418insA (HRAS)
ENST00000493230.5:c.*211_*212insA (HRAS) ENSP00000434023.1:n.*211_*212insA
NM_001130442.1:c.*180_*181insA (HRAS) NP_001123914.1:n.*180_*181insA
NM_005343.2:c.*72_*73insA (HRAS) NP_005334.1:n.*72_*73insA
NM_176795.3:c.*319_*320insA (HRAS) NP_789765.1:n.*319_*320insA
XM_011519875.1:c.-425+4118_-425+4119insT (LRRC56) XP_011518177.1:n.-425+4118_-425+4119insT
XM_011519877.1:c.-162+4118_-162+4119insT (LRRC56) XP_011518179.1:n.-162+4118_-162+4119insT
XR_242795.1:n.923_924insA (HRAS)
NM_001130442.2:c.*180_*181insA (HRAS) NP_001123914.1:n.*180_*181insA
NM_001318054.1:c.*72_*73insA (HRAS) NP_001304983.1:n.*72_*73insA
NM_005343.3:c.*72_*73insA (HRAS) NP_005334.1:n.*72_*73insA
NM_176795.4:c.*319_*320insA (HRAS) NP_789765.1:n.*319_*320insA
XM_011519875.2:c.-425+4118_-425+4119insT (LRRC56) XP_011518177.1:n.-425+4118_-425+4119insT
XM_011519877.2:c.-162+4118_-162+4119insT (LRRC56) XP_011518179.1:n.-162+4118_-162+4119insT
XM_017017167.1:c.-500+4118_-500+4119insT (LRRC56) XP_016872656.1:n.-500+4118_-500+4119insT
XM_017017168.1:c.-500+4118_-500+4119insT (LRRC56) XP_016872657.1:n.-500+4118_-500+4119insT
NM_005343.4:c.*72_*73insA (HRAS) MANE Select NP_005334.1:n.*72_*73insA
NM_001318054.2:c.*72_*73insA (HRAS) NP_001304983.1:n.*72_*73insA
NM_001130442.3:c.*180_*181insA (HRAS) NP_001123914.1:n.*180_*181insA
NM_176795.5:c.*319_*320insA (HRAS) MANE Plus Clinical NP_789765.1:n.*319_*320insA