Canonical Allele Identifier: CA180750

Gene: KRAS

Linked Data

• ClinVar Variation Id: 177777
• ClinVar RCV Id: RCV000154402 ; RCV000423236 ; RCV000440889
• dbSNP Id: rs121913238
• COSMIC: COSM549 ; COSM1159597
• MyVariant Identifiers: chr12:g.25380277G>T (hg19) ; chr12:g.25227343G>T (hg38)
• CIViC: CA180750
• PubMed: PMID:12460918 ; PMID:16361624 ; PMID:16618717 ; PMID:17384584 ; PMID:18316791 ; PMID:18794081 ; PMID:19047918 ; PMID:19114683 ; PMID:19255327 ; PMID:19679400 ; PMID:19773371 ; PMID:20921462 ; PMID:20921465 ; PMID:21228335 ; PMID:23406027 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227343G>T , CM000674.2:g.25227343G>T	GRCh38
NC_000012.11:g.25380277G>T , CM000674.1:g.25380277G>T	GRCh37
NC_000012.10:g.25271544G>T	NCBI36
NG_007524.1:g.28578C>A
NG_007524.2:g.28661C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17432C>A	ENSP00000452512.1:n.112-17432C>A
ENST00000685328.1:c.181C>A	ENSP00000508921.1:p.Gln61Lys
ENST00000686877.1:c.*152C>A	ENSP00000510431.1:n.*152C>A
ENST00000687356.1:c.112-1570C>A	ENSP00000510511.1:n.112-1570C>A
ENST00000688228.1:n.655C>A
ENST00000688940.1:c.181C>A	ENSP00000509238.1:p.Gln61Lys
ENST00000690804.1:c.*142C>A	ENSP00000508568.1:n.*142C>A
ENST00000692768.1:c.-18C>A	ENSP00000510254.1:n.-18C>A
ENST00000693229.1:c.112-6C>A	ENSP00000509223.1:n.112-6C>A
ENST00000256078.10:c.181C>A MANE Plus Clinical	ENSP00000256078.5:p.Gln61Lys
ENST00000311936.8:c.181C>A MANE Select	ENSP00000308495.3:p.Gln61Lys
ENST00000256078.8:c.181C>A	ENSP00000256078.4:p.Gln61Lys
ENST00000311936.7:c.181C>A	ENSP00000308495.3:p.Gln61Lys
ENST00000557334.5:c.112-17432C>A	ENSP00000452512.1:n.112-17432C>A
NM_004985.4:c.181C>A	NP_004976.2:p.Gln61Lys
NM_033360.3:c.181C>A	NP_203524.1:p.Gln61Lys
XM_006719069.2:c.181C>A	XP_006719132.1:p.Gln61Lys
XM_011520653.1:c.181C>A	XP_011518955.1:p.Gln61Lys
XM_006719069.4:c.181C>A	XP_006719132.1:p.Gln61Lys
XM_011520653.3:c.181C>A	XP_011518955.1:p.Gln61Lys
NM_001369786.1:c.181C>A	NP_001356715.1:p.Gln61Lys
NM_001369787.1:c.181C>A	NP_001356716.1:p.Gln61Lys
NM_004985.5:c.181C>A MANE Select	NP_004976.2:p.Gln61Lys
NM_033360.4:c.181C>A MANE Plus Clinical	NP_203524.1:p.Gln61Lys