Canonical Allele Identifier: CA2022884520

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209808C= , CM000674.2:g.25209808C=	GRCh38
NC_000012.11:g.25362742C= , CM000674.1:g.25362742C=	GRCh37
NC_000012.10:g.25254009C=	NCBI36
NG_007524.1:g.46113G=
NG_007524.2:g.46196G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.215G=	ENSP00000452512.1:p.Cys72=
ENST00000685328.1:c.554G=	ENSP00000508921.1:p.Cys185=
ENST00000686877.1:c.*525G=	ENSP00000510431.1:n.*525G=
ENST00000687356.1:c.*252G=	ENSP00000510511.1:n.*252G=
ENST00000688228.1:n.1028G=
ENST00000688940.1:c.554G=	ENSP00000509238.1:p.Cys185=
ENST00000690406.1:c.357G=
ENST00000690804.1:c.*515G=	ENSP00000508568.1:n.*515G=
ENST00000692768.1:c.356G=	ENSP00000510254.1:p.Cys119=
ENST00000693229.1:c.479G=	ENSP00000509223.1:p.Cys160=
ENST00000256078.10:c.*108G= MANE Plus Clinical	ENSP00000256078.5:n.*108G=
ENST00000311936.8:c.554G= MANE Select	ENSP00000308495.3:p.Cys185=
ENST00000256078.8:c.*108G=	ENSP00000256078.4:n.*108G=
ENST00000311936.7:c.554G=	ENSP00000308495.3:p.Cys185=
ENST00000557334.5:c.215G=	ENSP00000452512.1:p.Cys72=
NM_004985.4:c.554G=	NP_004976.2:p.Cys185=
NM_033360.3:c.*108G=	NP_203524.1:n.*108G=
XM_011520653.1:c.554G=	XP_011518955.1:p.Cys185=
XM_011520653.3:c.554G=	XP_011518955.1:p.Cys185=
NM_001369786.1:c.*108G=	NP_001356715.1:n.*108G=
NM_001369787.1:c.554G=	NP_001356716.1:p.Cys185=
NM_004985.5:c.554G= MANE Select	NP_004976.2:p.Cys185=
NM_033360.4:c.*108G= MANE Plus Clinical	NP_203524.1:n.*108G=