Canonical Allele Identifier: CA2022884646

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209871C= , CM000674.2:g.25209871C=	GRCh38
NC_000012.11:g.25362805C= , CM000674.1:g.25362805C=	GRCh37
NC_000012.10:g.25254072C=	NCBI36
NG_007524.1:g.46050G=
NG_007524.2:g.46133G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.152G=	ENSP00000452512.1:p.Arg51=
ENST00000685328.1:c.491G=	ENSP00000508921.1:p.Arg164=
ENST00000686877.1:c.*462G=	ENSP00000510431.1:n.*462G=
ENST00000687356.1:c.*189G=	ENSP00000510511.1:n.*189G=
ENST00000688228.1:n.965G=
ENST00000688940.1:c.491G=	ENSP00000509238.1:p.Arg164=
ENST00000690406.1:c.294G=
ENST00000690804.1:c.*452G=	ENSP00000508568.1:n.*452G=
ENST00000692768.1:c.293G=	ENSP00000510254.1:p.Arg98=
ENST00000693229.1:c.416G=	ENSP00000509223.1:p.Arg139=
ENST00000256078.10:c.*45G= MANE Plus Clinical	ENSP00000256078.5:n.*45G=
ENST00000311936.8:c.491G= MANE Select	ENSP00000308495.3:p.Arg164=
ENST00000256078.8:c.*45G=	ENSP00000256078.4:n.*45G=
ENST00000311936.7:c.491G=	ENSP00000308495.3:p.Arg164=
ENST00000557334.5:c.152G=	ENSP00000452512.1:p.Arg51=
NM_004985.4:c.491G=	NP_004976.2:p.Arg164=
NM_033360.3:c.*45G=	NP_203524.1:n.*45G=
XM_006719069.2:c.*45G=	XP_006719132.1:n.*45G=
XM_011520653.1:c.491G=	XP_011518955.1:p.Arg164=
XM_006719069.4:c.*45G=	XP_006719132.1:n.*45G=
XM_011520653.3:c.491G=	XP_011518955.1:p.Arg164=
NM_001369786.1:c.*45G=	NP_001356715.1:n.*45G=
NM_001369787.1:c.491G=	NP_001356716.1:p.Arg164=
NM_004985.5:c.491G= MANE Select	NP_004976.2:p.Arg164=
NM_033360.4:c.*45G= MANE Plus Clinical	NP_203524.1:n.*45G=