Canonical Allele Identifier: CA2022884716

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209900A= , CM000674.2:g.25209900A=	GRCh38
NC_000012.11:g.25362834A= , CM000674.1:g.25362834A=	GRCh37
NC_000012.10:g.25254101A=	NCBI36
NG_007524.1:g.46021T=
NG_007524.2:g.46104T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.123T=	ENSP00000452512.1:p.Asp41=
ENST00000685328.1:c.462T=	ENSP00000508921.1:p.Asp154=
ENST00000686877.1:c.*433T=	ENSP00000510431.1:n.*433T=
ENST00000687356.1:c.*160T=	ENSP00000510511.1:n.*160T=
ENST00000688228.1:n.936T=
ENST00000688940.1:c.462T=	ENSP00000509238.1:p.Asp154=
ENST00000690406.1:c.265T=
ENST00000690804.1:c.*423T=	ENSP00000508568.1:n.*423T=
ENST00000692768.1:c.264T=	ENSP00000510254.1:p.Asp88=
ENST00000693229.1:c.387T=	ENSP00000509223.1:p.Asp129=
ENST00000256078.10:c.*16T= MANE Plus Clinical	ENSP00000256078.5:n.*16T=
ENST00000311936.8:c.462T= MANE Select	ENSP00000308495.3:p.Asp154=
ENST00000256078.8:c.*16T=	ENSP00000256078.4:n.*16T=
ENST00000311936.7:c.462T=	ENSP00000308495.3:p.Asp154=
ENST00000557334.5:c.123T=	ENSP00000452512.1:p.Asp41=
NM_004985.4:c.462T=	NP_004976.2:p.Asp154=
NM_033360.3:c.*16T=	NP_203524.1:n.*16T=
XM_006719069.2:c.*16T=	XP_006719132.1:n.*16T=
XM_011520653.1:c.462T=	XP_011518955.1:p.Asp154=
XM_006719069.4:c.*16T=	XP_006719132.1:n.*16T=
XM_011520653.3:c.462T=	XP_011518955.1:p.Asp154=
NM_001369786.1:c.*16T=	NP_001356715.1:n.*16T=
NM_001369787.1:c.462T=	NP_001356716.1:p.Asp154=
NM_004985.5:c.462T= MANE Select	NP_004976.2:p.Asp154=
NM_033360.4:c.*16T= MANE Plus Clinical	NP_203524.1:n.*16T=