Canonical Allele Identifier: CA210876

Gene: KRAS

Linked Data

• ClinVar Variation Id: 45116
• ClinVar RCV Id: RCV000038258 ; RCV000202407 ; RCV000437806 ; RCV000443593 ; RCV000984128
• dbSNP Id: rs121913240
• COSMIC: COSM553 ; COSM1140131
• MyVariant Identifiers: chr12:g.25380276T>A (hg19) ; chr12:g.25227342T>A (hg38)
• CIViC: CA210876
• PubMed: PMID:12460918 ; PMID:15696205 ; PMID:16361624 ; PMID:16618717 ; PMID:17062680 ; PMID:17384584 ; PMID:18316791 ; PMID:18794081 ; PMID:19114683 ; PMID:19255327 ; PMID:19679400 ; PMID:19773371 ; PMID:20921462 ; PMID:20921465 ; PMID:21228335 ; PMID:23406027 ; PMID:25157968 ; PMID:27148585

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227342T>A , CM000674.2:g.25227342T>A	GRCh38
NC_000012.11:g.25380276T>A , CM000674.1:g.25380276T>A	GRCh37
NC_000012.10:g.25271543T>A	NCBI36
NG_007524.1:g.28579A>T
NG_007524.2:g.28662A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17431A>T	ENSP00000452512.1:n.112-17431A>T
ENST00000685328.1:c.182A>T	ENSP00000508921.1:p.Gln61Leu
ENST00000686877.1:c.*153A>T	ENSP00000510431.1:n.*153A>T
ENST00000687356.1:c.112-1569A>T	ENSP00000510511.1:n.112-1569A>T
ENST00000688228.1:n.656A>T
ENST00000688940.1:c.182A>T	ENSP00000509238.1:p.Gln61Leu
ENST00000690804.1:c.*143A>T	ENSP00000508568.1:n.*143A>T
ENST00000692768.1:c.-17A>T	ENSP00000510254.1:n.-17A>T
ENST00000693229.1:c.112-5A>T	ENSP00000509223.1:n.112-5A>T
ENST00000256078.10:c.182A>T MANE Plus Clinical	ENSP00000256078.5:p.Gln61Leu
ENST00000311936.8:c.182A>T MANE Select	ENSP00000308495.3:p.Gln61Leu
ENST00000256078.8:c.182A>T	ENSP00000256078.4:p.Gln61Leu
ENST00000311936.7:c.182A>T	ENSP00000308495.3:p.Gln61Leu
ENST00000557334.5:c.112-17431A>T	ENSP00000452512.1:n.112-17431A>T
NM_004985.4:c.182A>T	NP_004976.2:p.Gln61Leu
NM_033360.3:c.182A>T	NP_203524.1:p.Gln61Leu
XM_006719069.2:c.182A>T	XP_006719132.1:p.Gln61Leu
XM_011520653.1:c.182A>T	XP_011518955.1:p.Gln61Leu
XM_006719069.4:c.182A>T	XP_006719132.1:p.Gln61Leu
XM_011520653.3:c.182A>T	XP_011518955.1:p.Gln61Leu
NM_001369786.1:c.182A>T	NP_001356715.1:p.Gln61Leu
NM_001369787.1:c.182A>T	NP_001356716.1:p.Gln61Leu
NM_004985.5:c.182A>T MANE Select	NP_004976.2:p.Gln61Leu
NM_033360.4:c.182A>T MANE Plus Clinical	NP_203524.1:p.Gln61Leu