Canonical Allele Identifier: CA2022884515

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209806C= , CM000674.2:g.25209806C=	GRCh38
NC_000012.11:g.25362740C= , CM000674.1:g.25362740C=	GRCh37
NC_000012.10:g.25254007C=	NCBI36
NG_007524.1:g.46115G=
NG_007524.2:g.46198G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.217G=	ENSP00000452512.1:p.Val73=
ENST00000685328.1:c.556G=	ENSP00000508921.1:p.Val186=
ENST00000686877.1:c.*527G=	ENSP00000510431.1:n.*527G=
ENST00000687356.1:c.*254G=	ENSP00000510511.1:n.*254G=
ENST00000688228.1:n.1030G=
ENST00000688940.1:c.556G=	ENSP00000509238.1:p.Val186=
ENST00000690406.1:c.359G=
ENST00000690804.1:c.*517G=	ENSP00000508568.1:n.*517G=
ENST00000692768.1:c.358G=	ENSP00000510254.1:p.Val120=
ENST00000693229.1:c.481G=	ENSP00000509223.1:p.Val161=
ENST00000256078.10:c.*110G= MANE Plus Clinical	ENSP00000256078.5:n.*110G=
ENST00000311936.8:c.556G= MANE Select	ENSP00000308495.3:p.Val186=
ENST00000256078.8:c.*110G=	ENSP00000256078.4:n.*110G=
ENST00000311936.7:c.556G=	ENSP00000308495.3:p.Val186=
ENST00000557334.5:c.217G=	ENSP00000452512.1:p.Val73=
NM_004985.4:c.556G=	NP_004976.2:p.Val186=
NM_033360.3:c.*110G=	NP_203524.1:n.*110G=
XM_011520653.1:c.556G=	XP_011518955.1:p.Val186=
XM_011520653.3:c.556G=	XP_011518955.1:p.Val186=
NM_001369786.1:c.*110G=	NP_001356715.1:n.*110G=
NM_001369787.1:c.556G=	NP_001356716.1:p.Val186=
NM_004985.5:c.556G= MANE Select	NP_004976.2:p.Val186=
NM_033360.4:c.*110G= MANE Plus Clinical	NP_203524.1:n.*110G=