Canonical Allele Identifier: CA2022884479

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209771T= , CM000674.2:g.25209771T=	GRCh38
NC_000012.11:g.25362705T= , CM000674.1:g.25362705T=	GRCh37
NC_000012.10:g.25253972T=	NCBI36
NG_007524.1:g.46150A=
NG_007524.2:g.46233A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*24A=	ENSP00000452512.1:n.*24A=
ENST00000685328.1:c.*24A=	ENSP00000508921.1:n.*24A=
ENST00000686877.1:c.*562A=	ENSP00000510431.1:n.*562A=
ENST00000687356.1:c.*289A=	ENSP00000510511.1:n.*289A=
ENST00000688228.1:n.1065A=
ENST00000688940.1:c.*24A=	ENSP00000509238.1:n.*24A=
ENST00000690406.1:c.394A=
ENST00000690804.1:c.*552A=	ENSP00000508568.1:n.*552A=
ENST00000692768.1:c.*24A=	ENSP00000510254.1:n.*24A=
ENST00000693229.1:c.*24A=	ENSP00000509223.1:n.*24A=
ENST00000256078.10:c.*145A= MANE Plus Clinical	ENSP00000256078.5:n.*145A=
ENST00000311936.8:c.*24A= MANE Select	ENSP00000308495.3:n.*24A=
ENST00000256078.8:c.*145A=	ENSP00000256078.4:n.*145A=
ENST00000311936.7:c.*24A=	ENSP00000308495.3:n.*24A=
ENST00000557334.5:c.*24A=	ENSP00000452512.1:n.*24A=
NM_004985.4:c.*24A=	NP_004976.2:n.*24A=
NM_033360.3:c.*145A=	NP_203524.1:n.*145A=
XM_011520653.1:c.*24A=	XP_011518955.1:n.*24A=
XM_011520653.3:c.*24A=	XP_011518955.1:n.*24A=
NM_001369786.1:c.*145A=	NP_001356715.1:n.*145A=
NM_001369787.1:c.*24A=	NP_001356716.1:n.*24A=
NM_004985.5:c.*24A= MANE Select	NP_004976.2:n.*24A=
NM_033360.4:c.*145A= MANE Plus Clinical	NP_203524.1:n.*145A=