Canonical Allele Identifier: CA2022884666

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209875T= , CM000674.2:g.25209875T=	GRCh38
NC_000012.11:g.25362809T= , CM000674.1:g.25362809T=	GRCh37
NC_000012.10:g.25254076T=	NCBI36
NG_007524.1:g.46046A=
NG_007524.2:g.46129A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.148A=	ENSP00000452512.1:p.Ile50=
ENST00000685328.1:c.487A=	ENSP00000508921.1:p.Ile163=
ENST00000686877.1:c.*458A=	ENSP00000510431.1:n.*458A=
ENST00000687356.1:c.*185A=	ENSP00000510511.1:n.*185A=
ENST00000688228.1:n.961A=
ENST00000688940.1:c.487A=	ENSP00000509238.1:p.Ile163=
ENST00000690406.1:c.290A=
ENST00000690804.1:c.*448A=	ENSP00000508568.1:n.*448A=
ENST00000692768.1:c.289A=	ENSP00000510254.1:p.Ile97=
ENST00000693229.1:c.412A=	ENSP00000509223.1:p.Ile138=
ENST00000256078.10:c.*41A= MANE Plus Clinical	ENSP00000256078.5:n.*41A=
ENST00000311936.8:c.487A= MANE Select	ENSP00000308495.3:p.Ile163=
ENST00000256078.8:c.*41A=	ENSP00000256078.4:n.*41A=
ENST00000311936.7:c.487A=	ENSP00000308495.3:p.Ile163=
ENST00000557334.5:c.148A=	ENSP00000452512.1:p.Ile50=
NM_004985.4:c.487A=	NP_004976.2:p.Ile163=
NM_033360.3:c.*41A=	NP_203524.1:n.*41A=
XM_006719069.2:c.*41A=	XP_006719132.1:n.*41A=
XM_011520653.1:c.487A=	XP_011518955.1:p.Ile163=
XM_006719069.4:c.*41A=	XP_006719132.1:n.*41A=
XM_011520653.3:c.487A=	XP_011518955.1:p.Ile163=
NM_001369786.1:c.*41A=	NP_001356715.1:n.*41A=
NM_001369787.1:c.487A=	NP_001356716.1:p.Ile163=
NM_004985.5:c.487A= MANE Select	NP_004976.2:p.Ile163=
NM_033360.4:c.*41A= MANE Plus Clinical	NP_203524.1:n.*41A=