Canonical Allele Identifier: CA2022884490

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209776A= , CM000674.2:g.25209776A=	GRCh38
NC_000012.11:g.25362710A= , CM000674.1:g.25362710A=	GRCh37
NC_000012.10:g.25253977A=	NCBI36
NG_007524.1:g.46145T=
NG_007524.2:g.46228T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*19T=	ENSP00000452512.1:n.*19T=
ENST00000685328.1:c.*19T=	ENSP00000508921.1:n.*19T=
ENST00000686877.1:c.*557T=	ENSP00000510431.1:n.*557T=
ENST00000687356.1:c.*284T=	ENSP00000510511.1:n.*284T=
ENST00000688228.1:n.1060T=
ENST00000688940.1:c.*19T=	ENSP00000509238.1:n.*19T=
ENST00000690406.1:c.389T=
ENST00000690804.1:c.*547T=	ENSP00000508568.1:n.*547T=
ENST00000692768.1:c.*19T=	ENSP00000510254.1:n.*19T=
ENST00000693229.1:c.*19T=	ENSP00000509223.1:n.*19T=
ENST00000256078.10:c.*140T= MANE Plus Clinical	ENSP00000256078.5:n.*140T=
ENST00000311936.8:c.*19T= MANE Select	ENSP00000308495.3:n.*19T=
ENST00000256078.8:c.*140T=	ENSP00000256078.4:n.*140T=
ENST00000311936.7:c.*19T=	ENSP00000308495.3:n.*19T=
ENST00000557334.5:c.*19T=	ENSP00000452512.1:n.*19T=
NM_004985.4:c.*19T=	NP_004976.2:n.*19T=
NM_033360.3:c.*140T=	NP_203524.1:n.*140T=
XM_011520653.1:c.*19T=	XP_011518955.1:n.*19T=
XM_011520653.3:c.*19T=	XP_011518955.1:n.*19T=
NM_001369786.1:c.*140T=	NP_001356715.1:n.*140T=
NM_001369787.1:c.*19T=	NP_001356716.1:n.*19T=
NM_004985.5:c.*19T= MANE Select	NP_004976.2:n.*19T=
NM_033360.4:c.*140T= MANE Plus Clinical	NP_203524.1:n.*140T=