Canonical Allele Identifier: CA2022905960

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225641A= , CM000674.2:g.25225641A=	GRCh38
NC_000012.11:g.25378575A= , CM000674.1:g.25378575A=	GRCh37
NC_000012.10:g.25269842A=	NCBI36
NG_007524.1:g.30280T=
NG_007524.2:g.30363T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15730T=	ENSP00000452512.1:n.112-15730T=
ENST00000685328.1:c.423T=	ENSP00000508921.1:p.Phe141=
ENST00000686877.1:c.*394T=	ENSP00000510431.1:n.*394T=
ENST00000687356.1:c.*121T=	ENSP00000510511.1:n.*121T=
ENST00000688228.1:n.897T=
ENST00000688940.1:c.423T=	ENSP00000509238.1:p.Phe141=
ENST00000690406.1:c.133T=
ENST00000690804.1:c.*384T=	ENSP00000508568.1:n.*384T=
ENST00000692768.1:c.225T=	ENSP00000510254.1:p.Phe75=
ENST00000693229.1:c.348T=	ENSP00000509223.1:p.Phe116=
ENST00000256078.10:c.423T= MANE Plus Clinical	ENSP00000256078.5:p.Phe141=
ENST00000311936.8:c.423T= MANE Select	ENSP00000308495.3:p.Phe141=
ENST00000256078.8:c.423T=	ENSP00000256078.4:p.Phe141=
ENST00000311936.7:c.423T=	ENSP00000308495.3:p.Phe141=
ENST00000557334.5:c.112-15730T=	ENSP00000452512.1:n.112-15730T=
NM_004985.4:c.423T=	NP_004976.2:p.Phe141=
NM_033360.3:c.423T=	NP_203524.1:p.Phe141=
XM_006719069.2:c.423T=	XP_006719132.1:p.Phe141=
XM_011520653.1:c.423T=	XP_011518955.1:p.Phe141=
XM_006719069.4:c.423T=	XP_006719132.1:p.Phe141=
XM_011520653.3:c.423T=	XP_011518955.1:p.Phe141=
NM_001369786.1:c.423T=	NP_001356715.1:p.Phe141=
NM_001369787.1:c.423T=	NP_001356716.1:p.Phe141=
NM_004985.5:c.423T= MANE Select	NP_004976.2:p.Phe141=
NM_033360.4:c.423T= MANE Plus Clinical	NP_203524.1:p.Phe141=