Canonical Allele Identifier: CA472322509

Linked Data

gnomAD v4: 11-532735-G-A
MyVariant Identifiers: chr11:g.532735G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532735G>A , CM000673.2:g.532735G>A GRCh38
NC_000011.9:g.532735G>A , CM000673.1:g.532735G>A GRCh37
NC_000011.8:g.522735G>A NCBI36
NG_007666.1:g.7816C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-105C>T (HRAS) ENSP00000380722.3:n.*20-105C>T
ENST00000417302.7:c.*40C>T (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*40C>T
ENST00000397594.6:c.251-105C>T (HRAS) ENSP00000380722.2:n.251-105C>T
ENST00000417302.6:c.*40C>T (HRAS) ENSP00000388246.1:n.*40C>T
ENST00000462734.2:c.*83C>T (HRAS) ENSP00000507303.1:n.*83C>T
ENST00000311189.8:c.471C>T (HRAS) MANE Select ENSP00000309845.7:p.Tyr157=
ENST00000311189.7:c.471C>T (HRAS) ENSP00000309845.7:p.Tyr157=
ENST00000397594.5:c.*40C>T (HRAS) ENSP00000380722.1:n.*40C>T
ENST00000397596.6:c.471C>T (HRAS) ENSP00000380723.2:p.Tyr157=
ENST00000417302.5:c.*40C>T (HRAS) ENSP00000388246.1:n.*40C>T
ENST00000451590.5:c.471C>T (HRAS) ENSP00000407586.1:p.Tyr157=
ENST00000462734.1:n.246C>T (HRAS)
ENST00000478324.5:n.243-105C>T (HRAS)
ENST00000479482.1:n.392C>T (HRAS)
ENST00000493230.5:c.*40C>T (HRAS) ENSP00000434023.1:n.*40C>T
NM_001130442.1:c.471C>T (HRAS) NP_001123914.1:p.Tyr157=
NM_005343.2:c.471C>T (HRAS) NP_005334.1:p.Tyr157=
NM_176795.3:c.*40C>T (HRAS) NP_789765.1:n.*40C>T
XM_011519875.1:c.-425+4398G>A (LRRC56) XP_011518177.1:n.-425+4398G>A
XM_011519877.1:c.-162+4398G>A (LRRC56) XP_011518179.1:n.-162+4398G>A
XR_242795.1:n.752C>T (HRAS)
NM_001130442.2:c.471C>T (HRAS) NP_001123914.1:p.Tyr157=
NM_001318054.1:c.234C>T (HRAS) NP_001304983.1:p.Tyr78=
NM_005343.3:c.471C>T (HRAS) NP_005334.1:p.Tyr157=
NM_176795.4:c.*40C>T (HRAS) NP_789765.1:n.*40C>T
XM_011519875.2:c.-425+4398G>A (LRRC56) XP_011518177.1:n.-425+4398G>A
XM_011519877.2:c.-162+4398G>A (LRRC56) XP_011518179.1:n.-162+4398G>A
XM_017017167.1:c.-500+4398G>A (LRRC56) XP_016872656.1:n.-500+4398G>A
XM_017017168.1:c.-500+4398G>A (LRRC56) XP_016872657.1:n.-500+4398G>A
NM_005343.4:c.471C>T (HRAS) MANE Select NP_005334.1:p.Tyr157=
NM_001318054.2:c.234C>T (HRAS) NP_001304983.1:p.Tyr78=
NM_001130442.3:c.471C>T (HRAS) NP_001123914.1:p.Tyr157=
NM_176795.5:c.*40C>T (HRAS) MANE Plus Clinical NP_789765.1:n.*40C>T