Canonical Allele Identifier: CA234191

Gene: KRAS

Linked Data

• ClinVar Variation Id: 12594
• ClinVar RCV Id: RCV000013425 ; RCV000153427 ; RCV000623267 ; RCV000520745
• dbSNP Id: rs104894361
• COSMIC: COSM24602
• MyVariant Identifiers: chr12:g.25398304T>A (hg19) ; chr12:g.25245370T>A (hg38)
• ERepo: CA234191/MONDO:0018997/004
• PubMed: PMID:16773572 ; PMID:16825433 ; PMID:17056636 ; PMID:17704260 ; PMID:18386799 ; PMID:19467855 ; PMID:20949621 ; PMID:21062266 ; PMID:21063026 ; PMID:21079152 ; PMID:21396583 ; PMID:21784453 ; PMID:21797849 ; PMID:23891399 ; PMID:24240292 ; PMID:25180280 ; PMID:25644510 ; PMID:26249544

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245370T>A , CM000674.2:g.25245370T>A	GRCh38
NC_000012.11:g.25398304T>A , CM000674.1:g.25398304T>A	GRCh37
NC_000012.10:g.25289571T>A	NCBI36
NG_007524.1:g.10551A>T
NG_007524.2:g.10634A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.15A>T	ENSP00000451856.1:p.Lys5Asn
ENST00000557334.6:c.15A>T	ENSP00000452512.1:p.Lys5Asn
ENST00000685328.1:c.15A>T	ENSP00000508921.1:p.Lys5Asn
ENST00000686877.1:c.15A>T	ENSP00000510431.1:p.Lys5Asn
ENST00000686969.1:c.15A>T	ENSP00000510479.1:p.Lys5Asn
ENST00000687356.1:c.15A>T	ENSP00000510511.1:p.Lys5Asn
ENST00000688940.1:c.15A>T	ENSP00000509238.1:p.Lys5Asn
ENST00000690804.1:c.15A>T	ENSP00000508568.1:p.Lys5Asn
ENST00000692768.1:c.-88+5381A>T	ENSP00000510254.1:n.-88+5381A>T
ENST00000693229.1:c.15A>T	ENSP00000509223.1:p.Lys5Asn
ENST00000256078.10:c.15A>T MANE Plus Clinical	ENSP00000256078.5:p.Lys5Asn
ENST00000311936.8:c.15A>T MANE Select	ENSP00000308495.3:p.Lys5Asn
ENST00000256078.8:c.15A>T	ENSP00000256078.4:p.Lys5Asn
ENST00000311936.7:c.15A>T	ENSP00000308495.3:p.Lys5Asn
ENST00000556131.1:c.15A>T	ENSP00000451856.1:p.Lys5Asn
ENST00000557334.5:c.15A>T	ENSP00000452512.1:p.Lys5Asn
NM_004985.4:c.15A>T	NP_004976.2:p.Lys5Asn
NM_033360.3:c.15A>T	NP_203524.1:p.Lys5Asn
XM_006719069.2:c.15A>T	XP_006719132.1:p.Lys5Asn
XM_011520653.1:c.15A>T	XP_011518955.1:p.Lys5Asn
XM_006719069.4:c.15A>T	XP_006719132.1:p.Lys5Asn
XM_011520653.3:c.15A>T	XP_011518955.1:p.Lys5Asn
NM_001369786.1:c.15A>T	NP_001356715.1:p.Lys5Asn
NM_001369787.1:c.15A>T	NP_001356716.1:p.Lys5Asn
NM_004985.5:c.15A>T MANE Select	NP_004976.2:p.Lys5Asn
NM_033360.4:c.15A>T MANE Plus Clinical	NP_203524.1:p.Lys5Asn