Canonical Allele Identifier: CA122540

Gene: KRAS

Linked Data

• ClinVar Variation Id: 12583
• ClinVar RCV Id: RCV000013413 ; RCV000029216 ; RCV000150895 ; RCV000154262 ; RCV000157944 ; RCV000417765 ; RCV000439750 ; RCV000439101 ; RCV000585801 ; RCV000428010 ; RCV002291496 ; RCV003322589 ; RCV003539760 ; RCV003455987
• dbSNP Id: rs121913529
• gnomAD v2: 12-25398284-C-A
• gnomAD v4: 12-25245350-C-A
• COSMIC: COSM520 ; COSM1140133
• MyVariant Identifiers: chr12:g.25398284C>A (hg19) ; chr12:g.25245350C>A (hg38)
• PubMed: PMID:2278970 ; PMID:3122217 ; PMID:8439212 ; PMID:15696205 ; PMID:16361624 ; PMID:16434492 ; PMID:16618717 ; PMID:17332249 ; PMID:17384584 ; PMID:17704260 ; PMID:18316791 ; PMID:19018267 ; PMID:19047918 ; PMID:19075190 ; PMID:19114683 ; PMID:19255327 ; PMID:19358724 ; PMID:19679400 ; PMID:19773371 ; PMID:19881948 ; PMID:20609353 ; PMID:20921462 ; PMID:20921465 ; PMID:21169357 ; PMID:21228335 ; PMID:21398618 ; PMID:21975775 ; PMID:22235099 ; PMID:22407852 ; PMID:22683711 ; PMID:22897852 ; PMID:23096712 ; PMID:23406027 ; PMID:25157968 ; PMID:26372703 ; PMID:29298116
• CIViC: CA122540

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245350C>A , CM000674.2:g.25245350C>A	GRCh38
NC_000012.11:g.25398284C>A , CM000674.1:g.25398284C>A	GRCh37
NC_000012.10:g.25289551C>A	NCBI36
NG_007524.1:g.10571G>T
NG_007524.2:g.10654G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.35G>T	ENSP00000451856.1:p.Gly12Val
ENST00000557334.6:c.35G>T	ENSP00000452512.1:p.Gly12Val
ENST00000685328.1:c.35G>T	ENSP00000508921.1:p.Gly12Val
ENST00000686877.1:c.35G>T	ENSP00000510431.1:p.Gly12Val
ENST00000686969.1:c.35G>T	ENSP00000510479.1:p.Gly12Val
ENST00000687356.1:c.35G>T	ENSP00000510511.1:p.Gly12Val
ENST00000688940.1:c.35G>T	ENSP00000509238.1:p.Gly12Val
ENST00000690804.1:c.35G>T	ENSP00000508568.1:p.Gly12Val
ENST00000692768.1:c.-88+5401G>T	ENSP00000510254.1:n.-88+5401G>T
ENST00000693229.1:c.35G>T	ENSP00000509223.1:p.Gly12Val
ENST00000256078.10:c.35G>T MANE Plus Clinical	ENSP00000256078.5:p.Gly12Val
ENST00000311936.8:c.35G>T MANE Select	ENSP00000308495.3:p.Gly12Val
ENST00000256078.8:c.35G>T	ENSP00000256078.4:p.Gly12Val
ENST00000311936.7:c.35G>T	ENSP00000308495.3:p.Gly12Val
ENST00000556131.1:c.35G>T	ENSP00000451856.1:p.Gly12Val
ENST00000557334.5:c.35G>T	ENSP00000452512.1:p.Gly12Val
NM_004985.4:c.35G>T	NP_004976.2:p.Gly12Val
NM_033360.3:c.35G>T	NP_203524.1:p.Gly12Val
XM_006719069.2:c.35G>T	XP_006719132.1:p.Gly12Val
XM_011520653.1:c.35G>T	XP_011518955.1:p.Gly12Val
XM_006719069.4:c.35G>T	XP_006719132.1:p.Gly12Val
XM_011520653.3:c.35G>T	XP_011518955.1:p.Gly12Val
NM_001369786.1:c.35G>T	NP_001356715.1:p.Gly12Val
NM_001369787.1:c.35G>T	NP_001356716.1:p.Gly12Val
NM_004985.5:c.35G>T MANE Select	NP_004976.2:p.Gly12Val
NM_033360.4:c.35G>T MANE Plus Clinical	NP_203524.1:p.Gly12Val