Canonical Allele Identifier: CA2022905890

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225626T= , CM000674.2:g.25225626T=	GRCh38
NC_000012.11:g.25378560T= , CM000674.1:g.25378560T=	GRCh37
NC_000012.10:g.25269827T=	NCBI36
NG_007524.1:g.30295A=
NG_007524.2:g.30378A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15715A=	ENSP00000452512.1:n.112-15715A=
ENST00000685328.1:c.438A=	ENSP00000508921.1:p.Ala146=
ENST00000686877.1:c.*409A=	ENSP00000510431.1:n.*409A=
ENST00000687356.1:c.*136A=	ENSP00000510511.1:n.*136A=
ENST00000688228.1:n.912A=
ENST00000688940.1:c.438A=	ENSP00000509238.1:p.Ala146=
ENST00000690406.1:c.148A=
ENST00000690804.1:c.*399A=	ENSP00000508568.1:n.*399A=
ENST00000692768.1:c.240A=	ENSP00000510254.1:p.Ala80=
ENST00000693229.1:c.363A=	ENSP00000509223.1:p.Ala121=
ENST00000256078.10:c.438A= MANE Plus Clinical	ENSP00000256078.5:p.Ala146=
ENST00000311936.8:c.438A= MANE Select	ENSP00000308495.3:p.Ala146=
ENST00000256078.8:c.438A=	ENSP00000256078.4:p.Ala146=
ENST00000311936.7:c.438A=	ENSP00000308495.3:p.Ala146=
ENST00000557334.5:c.112-15715A=	ENSP00000452512.1:n.112-15715A=
NM_004985.4:c.438A=	NP_004976.2:p.Ala146=
NM_033360.3:c.438A=	NP_203524.1:p.Ala146=
XM_006719069.2:c.438A=	XP_006719132.1:p.Ala146=
XM_011520653.1:c.438A=	XP_011518955.1:p.Ala146=
XM_006719069.4:c.438A=	XP_006719132.1:p.Ala146=
XM_011520653.3:c.438A=	XP_011518955.1:p.Ala146=
NM_001369786.1:c.438A=	NP_001356715.1:p.Ala146=
NM_001369787.1:c.438A=	NP_001356716.1:p.Ala146=
NM_004985.5:c.438A= MANE Select	NP_004976.2:p.Ala146=
NM_033360.4:c.438A= MANE Plus Clinical	NP_203524.1:p.Ala146=