Canonical Allele Identifier: CA2022884392

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209676A= , CM000674.2:g.25209676A=	GRCh38
NC_000012.11:g.25362610A= , CM000674.1:g.25362610A=	GRCh37
NC_000012.10:g.25253877A=	NCBI36
NG_007524.1:g.46245T=
NG_007524.2:g.46328T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*119T=	ENSP00000452512.1:n.*119T=
ENST00000685328.1:c.*119T=	ENSP00000508921.1:n.*119T=
ENST00000686877.1:c.*657T=	ENSP00000510431.1:n.*657T=
ENST00000687356.1:c.*384T=	ENSP00000510511.1:n.*384T=
ENST00000688228.1:n.1160T=
ENST00000688940.1:c.*119T=	ENSP00000509238.1:n.*119T=
ENST00000690406.1:c.489T=
ENST00000690804.1:c.*647T=	ENSP00000508568.1:n.*647T=
ENST00000692768.1:c.*119T=	ENSP00000510254.1:n.*119T=
ENST00000693229.1:c.*119T=	ENSP00000509223.1:n.*119T=
ENST00000256078.10:c.*240T= MANE Plus Clinical	ENSP00000256078.5:n.*240T=
ENST00000311936.8:c.*119T= MANE Select	ENSP00000308495.3:n.*119T=
ENST00000256078.8:c.*240T=	ENSP00000256078.4:n.*240T=
ENST00000311936.7:c.*119T=	ENSP00000308495.3:n.*119T=
ENST00000557334.5:c.*119T=	ENSP00000452512.1:n.*119T=
NM_004985.4:c.*119T=	NP_004976.2:n.*119T=
NM_033360.3:c.*240T=	NP_203524.1:n.*240T=
XM_011520653.1:c.*119T=	XP_011518955.1:n.*119T=
XM_011520653.3:c.*119T=	XP_011518955.1:n.*119T=
NM_001369786.1:c.*240T=	NP_001356715.1:n.*240T=
NM_001369787.1:c.*119T=	NP_001356716.1:n.*119T=
NM_004985.5:c.*119T= MANE Select	NP_004976.2:n.*119T=
NM_033360.4:c.*240T= MANE Plus Clinical	NP_203524.1:n.*240T=