Canonical Allele Identifier: CA2022884690

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209888T= , CM000674.2:g.25209888T=	GRCh38
NC_000012.11:g.25362822T= , CM000674.1:g.25362822T=	GRCh37
NC_000012.10:g.25254089T=	NCBI36
NG_007524.1:g.46033A=
NG_007524.2:g.46116A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.135A=	ENSP00000452512.1:p.Thr45=
ENST00000685328.1:c.474A=	ENSP00000508921.1:p.Thr158=
ENST00000686877.1:c.*445A=	ENSP00000510431.1:n.*445A=
ENST00000687356.1:c.*172A=	ENSP00000510511.1:n.*172A=
ENST00000688228.1:n.948A=
ENST00000688940.1:c.474A=	ENSP00000509238.1:p.Thr158=
ENST00000690406.1:c.277A=
ENST00000690804.1:c.*435A=	ENSP00000508568.1:n.*435A=
ENST00000692768.1:c.276A=	ENSP00000510254.1:p.Thr92=
ENST00000693229.1:c.399A=	ENSP00000509223.1:p.Thr133=
ENST00000256078.10:c.*28A= MANE Plus Clinical	ENSP00000256078.5:n.*28A=
ENST00000311936.8:c.474A= MANE Select	ENSP00000308495.3:p.Thr158=
ENST00000256078.8:c.*28A=	ENSP00000256078.4:n.*28A=
ENST00000311936.7:c.474A=	ENSP00000308495.3:p.Thr158=
ENST00000557334.5:c.135A=	ENSP00000452512.1:p.Thr45=
NM_004985.4:c.474A=	NP_004976.2:p.Thr158=
NM_033360.3:c.*28A=	NP_203524.1:n.*28A=
XM_006719069.2:c.*28A=	XP_006719132.1:n.*28A=
XM_011520653.1:c.474A=	XP_011518955.1:p.Thr158=
XM_006719069.4:c.*28A=	XP_006719132.1:n.*28A=
XM_011520653.3:c.474A=	XP_011518955.1:p.Thr158=
NM_001369786.1:c.*28A=	NP_001356715.1:n.*28A=
NM_001369787.1:c.474A=	NP_001356716.1:p.Thr158=
NM_004985.5:c.474A= MANE Select	NP_004976.2:p.Thr158=
NM_033360.4:c.*28A= MANE Plus Clinical	NP_203524.1:n.*28A=