Canonical Allele Identifier: CA2611689690

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532772_532786dup , CM000673.2:g.532772_532786dup GRCh38
NC_000011.9:g.532772_532786dup , CM000673.1:g.532772_532786dup GRCh37
NC_000011.8:g.522772_522786dup NCBI36
NG_007666.1:g.7765_7779dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-156_*20-142dup (HRAS) ENSP00000380722.3:n.*20-156_*20-142dup
ENST00000417302.7:c.*20-31_*20-17dup (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*20-31_*20-17dup
ENST00000397594.6:c.251-156_251-142dup (HRAS) ENSP00000380722.2:n.251-156_251-142dup
ENST00000417302.6:c.*20-31_*20-17dup (HRAS) ENSP00000388246.1:n.*20-31_*20-17dup
ENST00000462734.2:c.*63-31_*63-17dup (HRAS) ENSP00000507303.1:n.*63-31_*63-17dup
ENST00000311189.8:c.451-31_451-17dup (HRAS) MANE Select ENSP00000309845.7:n.451-31_451-17dup
ENST00000311189.7:c.451-31_451-17dup (HRAS) ENSP00000309845.7:n.451-31_451-17dup
ENST00000397594.5:c.*20-31_*20-17dup (HRAS) ENSP00000380722.1:n.*20-31_*20-17dup
ENST00000397596.6:c.451-31_451-17dup (HRAS) ENSP00000380723.2:n.451-31_451-17dup
ENST00000417302.5:c.*20-31_*20-17dup (HRAS) ENSP00000388246.1:n.*20-31_*20-17dup
ENST00000451590.5:c.451-31_451-17dup (HRAS) ENSP00000407586.1:n.451-31_451-17dup
ENST00000462734.1:n.226-31_226-17dup (HRAS)
ENST00000478324.5:n.243-156_243-142dup (HRAS)
ENST00000479482.1:n.372-31_372-17dup (HRAS)
ENST00000493230.5:c.*20-31_*20-17dup (HRAS) ENSP00000434023.1:n.*20-31_*20-17dup
NM_001130442.1:c.451-31_451-17dup (HRAS) NP_001123914.1:n.451-31_451-17dup
NM_005343.2:c.451-31_451-17dup (HRAS) NP_005334.1:n.451-31_451-17dup
NM_176795.3:c.*20-31_*20-17dup (HRAS) NP_789765.1:n.*20-31_*20-17dup
XM_011519875.1:c.-425+4435_-425+4449dup (LRRC56) XP_011518177.1:n.-425+4435_-425+4449dup
XM_011519877.1:c.-162+4435_-162+4449dup (LRRC56) XP_011518179.1:n.-162+4435_-162+4449dup
XR_242795.1:n.732-31_732-17dup (HRAS)
NM_001130442.2:c.451-31_451-17dup (HRAS) NP_001123914.1:n.451-31_451-17dup
NM_001318054.1:c.214-31_214-17dup (HRAS) NP_001304983.1:n.214-31_214-17dup
NM_005343.3:c.451-31_451-17dup (HRAS) NP_005334.1:n.451-31_451-17dup
NM_176795.4:c.*20-31_*20-17dup (HRAS) NP_789765.1:n.*20-31_*20-17dup
XM_011519875.2:c.-425+4435_-425+4449dup (LRRC56) XP_011518177.1:n.-425+4435_-425+4449dup
XM_011519877.2:c.-162+4435_-162+4449dup (LRRC56) XP_011518179.1:n.-162+4435_-162+4449dup
XM_017017167.1:c.-500+4435_-500+4449dup (LRRC56) XP_016872656.1:n.-500+4435_-500+4449dup
XM_017017168.1:c.-500+4435_-500+4449dup (LRRC56) XP_016872657.1:n.-500+4435_-500+4449dup
NM_005343.4:c.451-31_451-17dup (HRAS) MANE Select NP_005334.1:n.451-31_451-17dup
NM_001318054.2:c.214-31_214-17dup (HRAS) NP_001304983.1:n.214-31_214-17dup
NM_001130442.3:c.451-31_451-17dup (HRAS) NP_001123914.1:n.451-31_451-17dup
NM_176795.5:c.*20-31_*20-17dup (HRAS) MANE Plus Clinical NP_789765.1:n.*20-31_*20-17dup