Canonical Allele Identifier: CA2978503551

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209897G>T , CM000674.2:g.25209897G>T	GRCh38
NC_000012.11:g.25362831G>T , CM000674.1:g.25362831G>T	GRCh37
NC_000012.10:g.25254098G>T	NCBI36
NG_007524.1:g.46024C>A
NG_007524.2:g.46107C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.126C>A	ENSP00000452512.1:p.Ala42=
ENST00000685328.1:c.465C>A	ENSP00000508921.1:p.Ala155=
ENST00000686877.1:c.*436C>A	ENSP00000510431.1:n.*436C>A
ENST00000687356.1:c.*163C>A	ENSP00000510511.1:n.*163C>A
ENST00000688228.1:n.939C>A
ENST00000688940.1:c.465C>A	ENSP00000509238.1:p.Ala155=
ENST00000690406.1:c.268C>A
ENST00000690804.1:c.*426C>A	ENSP00000508568.1:n.*426C>A
ENST00000692768.1:c.267C>A	ENSP00000510254.1:p.Ala89=
ENST00000693229.1:c.390C>A	ENSP00000509223.1:p.Ala130=
ENST00000256078.10:c.*19C>A MANE Plus Clinical	ENSP00000256078.5:n.*19C>A
ENST00000311936.8:c.465C>A MANE Select	ENSP00000308495.3:p.Ala155=
ENST00000256078.8:c.*19C>A	ENSP00000256078.4:n.*19C>A
ENST00000311936.7:c.465C>A	ENSP00000308495.3:p.Ala155=
ENST00000557334.5:c.126C>A	ENSP00000452512.1:p.Ala42=
NM_004985.4:c.465C>A	NP_004976.2:p.Ala155=
NM_033360.3:c.*19C>A	NP_203524.1:n.*19C>A
XM_006719069.2:c.*19C>A	XP_006719132.1:n.*19C>A
XM_011520653.1:c.465C>A	XP_011518955.1:p.Ala155=
XM_006719069.4:c.*19C>A	XP_006719132.1:n.*19C>A
XM_011520653.3:c.465C>A	XP_011518955.1:p.Ala155=
NM_001369786.1:c.*19C>A	NP_001356715.1:n.*19C>A
NM_001369787.1:c.465C>A	NP_001356716.1:p.Ala155=
NM_004985.5:c.465C>A MANE Select	NP_004976.2:p.Ala155=
NM_033360.4:c.*19C>A MANE Plus Clinical	NP_203524.1:n.*19C>A