Canonical Allele Identifier: CA2022884509

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209803T= , CM000674.2:g.25209803T=	GRCh38
NC_000012.11:g.25362737T= , CM000674.1:g.25362737T=	GRCh37
NC_000012.10:g.25254004T=	NCBI36
NG_007524.1:g.46118A=
NG_007524.2:g.46201A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.220A=	ENSP00000452512.1:p.Ile74=
ENST00000685328.1:c.559A=	ENSP00000508921.1:p.Ile187=
ENST00000686877.1:c.*530A=	ENSP00000510431.1:n.*530A=
ENST00000687356.1:c.*257A=	ENSP00000510511.1:n.*257A=
ENST00000688228.1:n.1033A=
ENST00000688940.1:c.559A=	ENSP00000509238.1:p.Ile187=
ENST00000690406.1:c.362A=
ENST00000690804.1:c.*520A=	ENSP00000508568.1:n.*520A=
ENST00000692768.1:c.361A=	ENSP00000510254.1:p.Ile121=
ENST00000693229.1:c.484A=	ENSP00000509223.1:p.Ile162=
ENST00000256078.10:c.*113A= MANE Plus Clinical	ENSP00000256078.5:n.*113A=
ENST00000311936.8:c.559A= MANE Select	ENSP00000308495.3:p.Ile187=
ENST00000256078.8:c.*113A=	ENSP00000256078.4:n.*113A=
ENST00000311936.7:c.559A=	ENSP00000308495.3:p.Ile187=
ENST00000557334.5:c.220A=	ENSP00000452512.1:p.Ile74=
NM_004985.4:c.559A=	NP_004976.2:p.Ile187=
NM_033360.3:c.*113A=	NP_203524.1:n.*113A=
XM_011520653.1:c.559A=	XP_011518955.1:p.Ile187=
XM_011520653.3:c.559A=	XP_011518955.1:p.Ile187=
NM_001369786.1:c.*113A=	NP_001356715.1:n.*113A=
NM_001369787.1:c.559A=	NP_001356716.1:p.Ile187=
NM_004985.5:c.559A= MANE Select	NP_004976.2:p.Ile187=
NM_033360.4:c.*113A= MANE Plus Clinical	NP_203524.1:n.*113A=