Canonical Allele Identifier: CA16602445
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375968
dbSNP Id: rs121913535
COSMIC: COSM528

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25245348C>T , CM000674.2:g.25245348C>T GRCh38
NC_000012.11:g.25398282C>T , CM000674.1:g.25398282C>T GRCh37
NC_000012.10:g.25289549C>T NCBI36
NG_007524.1:g.10573G>A
NG_007524.2:g.10656G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000556131.2:c.37G>A ENSP00000451856.1:p.Gly13Ser
ENST00000557334.6:c.37G>A ENSP00000452512.1:p.Gly13Ser
ENST00000685328.1:c.37G>A ENSP00000508921.1:p.Gly13Ser
ENST00000686877.1:c.37G>A ENSP00000510431.1:p.Gly13Ser
ENST00000686969.1:c.37G>A ENSP00000510479.1:p.Gly13Ser
ENST00000687356.1:c.37G>A ENSP00000510511.1:p.Gly13Ser
ENST00000688940.1:c.37G>A ENSP00000509238.1:p.Gly13Ser
ENST00000690804.1:c.37G>A ENSP00000508568.1:p.Gly13Ser
ENST00000692768.1:c.-88+5403G>A ENSP00000510254.1:n.-88+5403G>A
ENST00000693229.1:c.37G>A ENSP00000509223.1:p.Gly13Ser
ENST00000256078.10:c.37G>A MANE Plus Clinical ENSP00000256078.5:p.Gly13Ser
ENST00000311936.8:c.37G>A MANE Select ENSP00000308495.3:p.Gly13Ser
ENST00000256078.8:c.37G>A ENSP00000256078.4:p.Gly13Ser
ENST00000311936.7:c.37G>A ENSP00000308495.3:p.Gly13Ser
ENST00000556131.1:c.37G>A ENSP00000451856.1:p.Gly13Ser
ENST00000557334.5:c.37G>A ENSP00000452512.1:p.Gly13Ser
NM_004985.4:c.37G>A NP_004976.2:p.Gly13Ser
NM_033360.3:c.37G>A NP_203524.1:p.Gly13Ser
XM_006719069.2:c.37G>A XP_006719132.1:p.Gly13Ser
XM_011520653.1:c.37G>A XP_011518955.1:p.Gly13Ser
XM_006719069.4:c.37G>A XP_006719132.1:p.Gly13Ser
XM_011520653.3:c.37G>A XP_011518955.1:p.Gly13Ser
NM_001369786.1:c.37G>A NP_001356715.1:p.Gly13Ser
NM_001369787.1:c.37G>A NP_001356716.1:p.Gly13Ser
NM_004985.5:c.37G>A MANE Select NP_004976.2:p.Gly13Ser
NM_033360.4:c.37G>A MANE Plus Clinical NP_203524.1:p.Gly13Ser