Canonical Allele Identifier: CA2611691456

Linked Data

gnomAD v4: 11-532374-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532374T>A , CM000673.2:g.532374T>A GRCh38
NC_000011.9:g.532374T>A , CM000673.1:g.532374T>A GRCh37
NC_000011.8:g.522374T>A NCBI36
NG_007666.1:g.8177A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*276A>T (HRAS) ENSP00000380722.3:n.*276A>T
ENST00000417302.7:c.*401A>T (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*401A>T
ENST00000397594.6:c.507A>T (HRAS) ENSP00000380722.2:n.507A>T
ENST00000417302.6:c.*401A>T (HRAS) ENSP00000388246.1:n.*401A>T
ENST00000462734.2:c.*336A>T (HRAS) ENSP00000507303.1:n.*336A>T
ENST00000311189.8:c.*154A>T (HRAS) MANE Select ENSP00000309845.7:n.*154A>T
ENST00000397594.5:c.*401A>T (HRAS) ENSP00000380722.1:n.*401A>T
ENST00000397596.6:c.*262A>T (HRAS) ENSP00000380723.2:n.*262A>T
ENST00000417302.5:c.*401A>T (HRAS) ENSP00000388246.1:n.*401A>T
ENST00000451590.5:c.*262A>T (HRAS) ENSP00000407586.1:n.*262A>T
ENST00000462734.1:n.499A>T (HRAS)
ENST00000478324.5:n.499A>T (HRAS)
ENST00000493230.5:c.*293A>T (HRAS) ENSP00000434023.1:n.*293A>T
NM_001130442.1:c.*262A>T (HRAS) NP_001123914.1:n.*262A>T
NM_005343.2:c.*154A>T (HRAS) NP_005334.1:n.*154A>T
NM_176795.3:c.*401A>T (HRAS) NP_789765.1:n.*401A>T
XM_011519875.1:c.-425+4037T>A (LRRC56) XP_011518177.1:n.-425+4037T>A
XM_011519877.1:c.-162+4037T>A (LRRC56) XP_011518179.1:n.-162+4037T>A
XR_242795.1:n.1005A>T (HRAS)
NM_001130442.2:c.*262A>T (HRAS) NP_001123914.1:n.*262A>T
NM_001318054.1:c.*154A>T (HRAS) NP_001304983.1:n.*154A>T
NM_005343.3:c.*154A>T (HRAS) NP_005334.1:n.*154A>T
NM_176795.4:c.*401A>T (HRAS) NP_789765.1:n.*401A>T
XM_011519875.2:c.-425+4037T>A (LRRC56) XP_011518177.1:n.-425+4037T>A
XM_011519877.2:c.-162+4037T>A (LRRC56) XP_011518179.1:n.-162+4037T>A
XM_017017167.1:c.-500+4037T>A (LRRC56) XP_016872656.1:n.-500+4037T>A
XM_017017168.1:c.-500+4037T>A (LRRC56) XP_016872657.1:n.-500+4037T>A
NM_005343.4:c.*154A>T (HRAS) MANE Select NP_005334.1:n.*154A>T
NM_001318054.2:c.*154A>T (HRAS) NP_001304983.1:n.*154A>T
NM_001130442.3:c.*262A>T (HRAS) NP_001123914.1:n.*262A>T
NM_176795.5:c.*401A>T (HRAS) MANE Plus Clinical NP_789765.1:n.*401A>T