Canonical Allele Identifier: CA2022905904

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225627G= , CM000674.2:g.25225627G=	GRCh38
NC_000012.11:g.25378561G= , CM000674.1:g.25378561G=	GRCh37
NC_000012.10:g.25269828G=	NCBI36
NG_007524.1:g.30294C=
NG_007524.2:g.30377C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15716C=	ENSP00000452512.1:n.112-15716C=
ENST00000685328.1:c.437C=	ENSP00000508921.1:p.Ala146=
ENST00000686877.1:c.*408C=	ENSP00000510431.1:n.*408C=
ENST00000687356.1:c.*135C=	ENSP00000510511.1:n.*135C=
ENST00000688228.1:n.911C=
ENST00000688940.1:c.437C=	ENSP00000509238.1:p.Ala146=
ENST00000690406.1:c.147C=
ENST00000690804.1:c.*398C=	ENSP00000508568.1:n.*398C=
ENST00000692768.1:c.239C=	ENSP00000510254.1:p.Ala80=
ENST00000693229.1:c.362C=	ENSP00000509223.1:p.Ala121=
ENST00000256078.10:c.437C= MANE Plus Clinical	ENSP00000256078.5:p.Ala146=
ENST00000311936.8:c.437C= MANE Select	ENSP00000308495.3:p.Ala146=
ENST00000256078.8:c.437C=	ENSP00000256078.4:p.Ala146=
ENST00000311936.7:c.437C=	ENSP00000308495.3:p.Ala146=
ENST00000557334.5:c.112-15716C=	ENSP00000452512.1:n.112-15716C=
NM_004985.4:c.437C=	NP_004976.2:p.Ala146=
NM_033360.3:c.437C=	NP_203524.1:p.Ala146=
XM_006719069.2:c.437C=	XP_006719132.1:p.Ala146=
XM_011520653.1:c.437C=	XP_011518955.1:p.Ala146=
XM_006719069.4:c.437C=	XP_006719132.1:p.Ala146=
XM_011520653.3:c.437C=	XP_011518955.1:p.Ala146=
NM_001369786.1:c.437C=	NP_001356715.1:p.Ala146=
NM_001369787.1:c.437C=	NP_001356716.1:p.Ala146=
NM_004985.5:c.437C= MANE Select	NP_004976.2:p.Ala146=
NM_033360.4:c.437C= MANE Plus Clinical	NP_203524.1:p.Ala146=