Canonical Allele Identifier: CA2022884502

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209798C= , CM000674.2:g.25209798C=	GRCh38
NC_000012.11:g.25362732C= , CM000674.1:g.25362732C=	GRCh37
NC_000012.10:g.25253999C=	NCBI36
NG_007524.1:g.46123G=
NG_007524.2:g.46206G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.225G=	ENSP00000452512.1:p.Met75=
ENST00000685328.1:c.564G=	ENSP00000508921.1:p.Met188=
ENST00000686877.1:c.*535G=	ENSP00000510431.1:n.*535G=
ENST00000687356.1:c.*262G=	ENSP00000510511.1:n.*262G=
ENST00000688228.1:n.1038G=
ENST00000688940.1:c.564G=	ENSP00000509238.1:p.Met188=
ENST00000690406.1:c.367G=
ENST00000690804.1:c.*525G=	ENSP00000508568.1:n.*525G=
ENST00000692768.1:c.366G=	ENSP00000510254.1:p.Met122=
ENST00000693229.1:c.489G=	ENSP00000509223.1:p.Met163=
ENST00000256078.10:c.*118G= MANE Plus Clinical	ENSP00000256078.5:n.*118G=
ENST00000311936.8:c.564G= MANE Select	ENSP00000308495.3:p.Met188=
ENST00000256078.8:c.*118G=	ENSP00000256078.4:n.*118G=
ENST00000311936.7:c.564G=	ENSP00000308495.3:p.Met188=
ENST00000557334.5:c.225G=	ENSP00000452512.1:p.Met75=
NM_004985.4:c.564G=	NP_004976.2:p.Met188=
NM_033360.3:c.*118G=	NP_203524.1:n.*118G=
XM_011520653.1:c.564G=	XP_011518955.1:p.Met188=
XM_011520653.3:c.564G=	XP_011518955.1:p.Met188=
NM_001369786.1:c.*118G=	NP_001356715.1:n.*118G=
NM_001369787.1:c.564G=	NP_001356716.1:p.Met188=
NM_004985.5:c.564G= MANE Select	NP_004976.2:p.Met188=
NM_033360.4:c.*118G= MANE Plus Clinical	NP_203524.1:n.*118G=