Canonical Allele Identifier: CA2022884707

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209896A= , CM000674.2:g.25209896A=	GRCh38
NC_000012.11:g.25362830A= , CM000674.1:g.25362830A=	GRCh37
NC_000012.10:g.25254097A=	NCBI36
NG_007524.1:g.46025T=
NG_007524.2:g.46108T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.127T=	ENSP00000452512.1:p.Phe43=
ENST00000685328.1:c.466T=	ENSP00000508921.1:p.Phe156=
ENST00000686877.1:c.*437T=	ENSP00000510431.1:n.*437T=
ENST00000687356.1:c.*164T=	ENSP00000510511.1:n.*164T=
ENST00000688228.1:n.940T=
ENST00000688940.1:c.466T=	ENSP00000509238.1:p.Phe156=
ENST00000690406.1:c.269T=
ENST00000690804.1:c.*427T=	ENSP00000508568.1:n.*427T=
ENST00000692768.1:c.268T=	ENSP00000510254.1:p.Phe90=
ENST00000693229.1:c.391T=	ENSP00000509223.1:p.Phe131=
ENST00000256078.10:c.*20T= MANE Plus Clinical	ENSP00000256078.5:n.*20T=
ENST00000311936.8:c.466T= MANE Select	ENSP00000308495.3:p.Phe156=
ENST00000256078.8:c.*20T=	ENSP00000256078.4:n.*20T=
ENST00000311936.7:c.466T=	ENSP00000308495.3:p.Phe156=
ENST00000557334.5:c.127T=	ENSP00000452512.1:p.Phe43=
NM_004985.4:c.466T=	NP_004976.2:p.Phe156=
NM_033360.3:c.*20T=	NP_203524.1:n.*20T=
XM_006719069.2:c.*20T=	XP_006719132.1:n.*20T=
XM_011520653.1:c.466T=	XP_011518955.1:p.Phe156=
XM_006719069.4:c.*20T=	XP_006719132.1:n.*20T=
XM_011520653.3:c.466T=	XP_011518955.1:p.Phe156=
NM_001369786.1:c.*20T=	NP_001356715.1:n.*20T=
NM_001369787.1:c.466T=	NP_001356716.1:p.Phe156=
NM_004985.5:c.466T= MANE Select	NP_004976.2:p.Phe156=
NM_033360.4:c.*20T= MANE Plus Clinical	NP_203524.1:n.*20T=