Canonical Allele Identifier: CA122531

Gene: KRAS

Linked Data

• ClinVar Variation Id: 12579
• ClinVar RCV Id: RCV000013407 ; RCV000013408 ; RCV000154401 ; RCV000422773 ; RCV000433472 ; RCV000441777 ; RCV000585776 ; RCV001356365 ; RCV002513010
• dbSNP Id: rs121913530
• gnomAD v2: 12-25398285-C-G
• COSMIC: COSM518 ; COSM1157797
• MyVariant Identifiers: chr12:g.25398285C>G (hg19) ; chr12:g.25245351C>G (hg38)
• CIViC: CA122531
• PubMed: PMID:6695174 ; PMID:12460918 ; PMID:15696205 ; PMID:16361624 ; PMID:16618717 ; PMID:17384584 ; PMID:18316791 ; PMID:18794081 ; PMID:19018267 ; PMID:19114683 ; PMID:19255327 ; PMID:19679400 ; PMID:19773371 ; PMID:20921462 ; PMID:20921465 ; PMID:21228335 ; PMID:21975775 ; PMID:22722830 ; PMID:23182985 ; PMID:23406027 ; PMID:25157968 ; PMID:29610392

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245351C>G , CM000674.2:g.25245351C>G	GRCh38
NC_000012.11:g.25398285C>G , CM000674.1:g.25398285C>G	GRCh37
NC_000012.10:g.25289552C>G	NCBI36
NG_007524.1:g.10570G>C
NG_007524.2:g.10653G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.34G>C	ENSP00000451856.1:p.Gly12Arg
ENST00000557334.6:c.34G>C	ENSP00000452512.1:p.Gly12Arg
ENST00000685328.1:c.34G>C	ENSP00000508921.1:p.Gly12Arg
ENST00000686877.1:c.34G>C	ENSP00000510431.1:p.Gly12Arg
ENST00000686969.1:c.34G>C	ENSP00000510479.1:p.Gly12Arg
ENST00000687356.1:c.34G>C	ENSP00000510511.1:p.Gly12Arg
ENST00000688940.1:c.34G>C	ENSP00000509238.1:p.Gly12Arg
ENST00000690804.1:c.34G>C	ENSP00000508568.1:p.Gly12Arg
ENST00000692768.1:c.-88+5400G>C	ENSP00000510254.1:n.-88+5400G>C
ENST00000693229.1:c.34G>C	ENSP00000509223.1:p.Gly12Arg
ENST00000256078.10:c.34G>C MANE Plus Clinical	ENSP00000256078.5:p.Gly12Arg
ENST00000311936.8:c.34G>C MANE Select	ENSP00000308495.3:p.Gly12Arg
ENST00000256078.8:c.34G>C	ENSP00000256078.4:p.Gly12Arg
ENST00000311936.7:c.34G>C	ENSP00000308495.3:p.Gly12Arg
ENST00000556131.1:c.34G>C	ENSP00000451856.1:p.Gly12Arg
ENST00000557334.5:c.34G>C	ENSP00000452512.1:p.Gly12Arg
NM_004985.4:c.34G>C	NP_004976.2:p.Gly12Arg
NM_033360.3:c.34G>C	NP_203524.1:p.Gly12Arg
XM_006719069.2:c.34G>C	XP_006719132.1:p.Gly12Arg
XM_011520653.1:c.34G>C	XP_011518955.1:p.Gly12Arg
XM_006719069.4:c.34G>C	XP_006719132.1:p.Gly12Arg
XM_011520653.3:c.34G>C	XP_011518955.1:p.Gly12Arg
NM_001369786.1:c.34G>C	NP_001356715.1:p.Gly12Arg
NM_001369787.1:c.34G>C	NP_001356716.1:p.Gly12Arg
NM_004985.5:c.34G>C MANE Select	NP_004976.2:p.Gly12Arg
NM_033360.4:c.34G>C MANE Plus Clinical	NP_203524.1:p.Gly12Arg