Canonical Allele Identifier: CA2022884601

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209843A= , CM000674.2:g.25209843A=	GRCh38
NC_000012.11:g.25362777A= , CM000674.1:g.25362777A=	GRCh37
NC_000012.10:g.25254044A=	NCBI36
NG_007524.1:g.46078T=
NG_007524.2:g.46161T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.180T=	ENSP00000452512.1:p.Asp60=
ENST00000685328.1:c.519T=	ENSP00000508921.1:p.Asp173=
ENST00000686877.1:c.*490T=	ENSP00000510431.1:n.*490T=
ENST00000687356.1:c.*217T=	ENSP00000510511.1:n.*217T=
ENST00000688228.1:n.993T=
ENST00000688940.1:c.519T=	ENSP00000509238.1:p.Asp173=
ENST00000690406.1:c.322T=
ENST00000690804.1:c.*480T=	ENSP00000508568.1:n.*480T=
ENST00000692768.1:c.321T=	ENSP00000510254.1:p.Asp107=
ENST00000693229.1:c.444T=	ENSP00000509223.1:p.Asp148=
ENST00000256078.10:c.*73T= MANE Plus Clinical	ENSP00000256078.5:n.*73T=
ENST00000311936.8:c.519T= MANE Select	ENSP00000308495.3:p.Asp173=
ENST00000256078.8:c.*73T=	ENSP00000256078.4:n.*73T=
ENST00000311936.7:c.519T=	ENSP00000308495.3:p.Asp173=
ENST00000557334.5:c.180T=	ENSP00000452512.1:p.Asp60=
NM_004985.4:c.519T=	NP_004976.2:p.Asp173=
NM_033360.3:c.*73T=	NP_203524.1:n.*73T=
XM_006719069.2:c.*73T=	XP_006719132.1:n.*73T=
XM_011520653.1:c.519T=	XP_011518955.1:p.Asp173=
XM_006719069.4:c.*73T=	XP_006719132.1:n.*73T=
XM_011520653.3:c.519T=	XP_011518955.1:p.Asp173=
NM_001369786.1:c.*73T=	NP_001356715.1:n.*73T=
NM_001369787.1:c.519T=	NP_001356716.1:p.Asp173=
NM_004985.5:c.519T= MANE Select	NP_004976.2:p.Asp173=
NM_033360.4:c.*73T= MANE Plus Clinical	NP_203524.1:n.*73T=