Canonical Allele Identifier: CA256478
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12587
dbSNP Id: rs104894360

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209904T>A , CM000674.2:g.25209904T>A GRCh38
NC_000012.11:g.25362838T>A , CM000674.1:g.25362838T>A GRCh37
NC_000012.10:g.25254105T>A NCBI36
NG_007524.1:g.46017A>T
NG_007524.2:g.46100A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.*12A>T ENSP00000256078.5:p.=
ENST00000311936.8:c.458A>T MANE Select ENSP00000308495.3:p.Asp153Val
ENST00000256078.8:c.*12A>T ENSP00000256078.4:p.=
ENST00000311936.7:c.458A>T ENSP00000308495.3:p.Asp153Val
ENST00000557334.5:c.119A>T ENSP00000452512.1:p.Asp40Val
NM_004985.4:c.458A>T NP_004976.2:p.Asp153Val
NM_033360.3:c.*12A>T NP_203524.1:p.=
XM_006719069.2:c.*12A>T XP_006719132.1:p.=
XM_011520653.1:c.458A>T XP_011518955.1:p.Asp153Val
XM_006719069.4:c.*12A>T XP_006719132.1:p.=
XM_011520653.3:c.458A>T XP_011518955.1:p.Asp153Val
NM_001369786.1:c.*12A>T NP_001356715.1:p.=
NM_001369787.1:c.458A>T NP_001356716.1:p.Asp153Val
NM_004985.5:c.458A>T MANE Select NP_004976.2:p.Asp153Val
NM_033360.4:c.*12A>T NP_203524.1:p.=