Canonical Allele Identifier: CA2022884611

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209854T= , CM000674.2:g.25209854T=	GRCh38
NC_000012.11:g.25362788T= , CM000674.1:g.25362788T=	GRCh37
NC_000012.10:g.25254055T=	NCBI36
NG_007524.1:g.46067A=
NG_007524.2:g.46150A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.169A=	ENSP00000452512.1:p.Met57=
ENST00000685328.1:c.508A=	ENSP00000508921.1:p.Met170=
ENST00000686877.1:c.*479A=	ENSP00000510431.1:n.*479A=
ENST00000687356.1:c.*206A=	ENSP00000510511.1:n.*206A=
ENST00000688228.1:n.982A=
ENST00000688940.1:c.508A=	ENSP00000509238.1:p.Met170=
ENST00000690406.1:c.311A=
ENST00000690804.1:c.*469A=	ENSP00000508568.1:n.*469A=
ENST00000692768.1:c.310A=	ENSP00000510254.1:p.Met104=
ENST00000693229.1:c.433A=	ENSP00000509223.1:p.Met145=
ENST00000256078.10:c.*62A= MANE Plus Clinical	ENSP00000256078.5:n.*62A=
ENST00000311936.8:c.508A= MANE Select	ENSP00000308495.3:p.Met170=
ENST00000256078.8:c.*62A=	ENSP00000256078.4:n.*62A=
ENST00000311936.7:c.508A=	ENSP00000308495.3:p.Met170=
ENST00000557334.5:c.169A=	ENSP00000452512.1:p.Met57=
NM_004985.4:c.508A=	NP_004976.2:p.Met170=
NM_033360.3:c.*62A=	NP_203524.1:n.*62A=
XM_006719069.2:c.*62A=	XP_006719132.1:n.*62A=
XM_011520653.1:c.508A=	XP_011518955.1:p.Met170=
XM_006719069.4:c.*62A=	XP_006719132.1:n.*62A=
XM_011520653.3:c.508A=	XP_011518955.1:p.Met170=
NM_001369786.1:c.*62A=	NP_001356715.1:n.*62A=
NM_001369787.1:c.508A=	NP_001356716.1:p.Met170=
NM_004985.5:c.508A= MANE Select	NP_004976.2:p.Met170=
NM_033360.4:c.*62A= MANE Plus Clinical	NP_203524.1:n.*62A=