Canonical Allele Identifier: CA135576
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 45125
dbSNP Id: rs397517040

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245346G>A , CM000674.2:g.25245346G>A GRCh38
NC_000012.11:g.25398280G>A , CM000674.1:g.25398280G>A GRCh37
NC_000012.10:g.25289547G>A NCBI36
NG_007524.1:g.10575C>T
NG_007524.2:g.10658C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.39C>T ENSP00000256078.5:p.Gly13=
ENST00000311936.8:c.39C>T MANE Select ENSP00000308495.3:p.Gly13=
ENST00000256078.8:c.39C>T ENSP00000256078.4:p.Gly13=
ENST00000311936.7:c.39C>T ENSP00000308495.3:p.Gly13=
ENST00000556131.1:c.39C>T ENSP00000451856.1:p.Gly13=
ENST00000557334.5:c.39C>T ENSP00000452512.1:p.Gly13=
NM_004985.4:c.39C>T NP_004976.2:p.Gly13=
NM_033360.3:c.39C>T NP_203524.1:p.Gly13=
XM_006719069.2:c.39C>T XP_006719132.1:p.Gly13=
XM_011520653.1:c.39C>T XP_011518955.1:p.Gly13=
XM_006719069.4:c.39C>T XP_006719132.1:p.Gly13=
XM_011520653.3:c.39C>T XP_011518955.1:p.Gly13=
NM_001369786.1:c.39C>T NP_001356715.1:p.Gly13=
NM_001369787.1:c.39C>T NP_001356716.1:p.Gly13=
NM_004985.5:c.39C>T MANE Select NP_004976.2:p.Gly13=
NM_033360.4:c.39C>T NP_203524.1:p.Gly13=