Canonical Allele Identifier: CA135552

Gene: KRAS

Linked Data

• ClinVar Variation Id: 45117
• ClinVar RCV Id: RCV000038259 ; RCV000420404 ; RCV000433108 ; RCV000440092 ; RCV000445124 ; RCV000417543 ; RCV000421965 ; RCV000423952 ; RCV000433564 ; RCV000430651 ; RCV000441804 ; RCV000423293 ; RCV000429878 ; RCV000435442 ; RCV003445113
• dbSNP Id: rs17851045
• COSMIC: COSM555 ; COSM1146992
• MyVariant Identifiers: chr12:g.25380275T>A (hg19) ; chr12:g.25227341T>A (hg38)
• PubMed: PMID:2278970 ; PMID:3122217 ; PMID:12460918 ; PMID:15696205 ; PMID:16361624 ; PMID:16434492 ; PMID:16618717 ; PMID:18316791 ; PMID:18794081 ; PMID:19075190 ; PMID:19114683 ; PMID:19679400 ; PMID:20921462 ; PMID:20921465 ; PMID:21228335 ; PMID:22407852 ; PMID:22722830 ; PMID:23325582 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227341T>A , CM000674.2:g.25227341T>A	GRCh38
NC_000012.11:g.25380275T>A , CM000674.1:g.25380275T>A	GRCh37
NC_000012.10:g.25271542T>A	NCBI36
NG_007524.1:g.28580A>T
NG_007524.2:g.28663A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17430A>T	ENSP00000452512.1:n.112-17430A>T
ENST00000685328.1:c.183A>T	ENSP00000508921.1:p.Gln61His
ENST00000686877.1:c.*154A>T	ENSP00000510431.1:n.*154A>T
ENST00000687356.1:c.112-1568A>T	ENSP00000510511.1:n.112-1568A>T
ENST00000688228.1:n.657A>T
ENST00000688940.1:c.183A>T	ENSP00000509238.1:p.Gln61His
ENST00000690804.1:c.*144A>T	ENSP00000508568.1:n.*144A>T
ENST00000692768.1:c.-16A>T	ENSP00000510254.1:n.-16A>T
ENST00000693229.1:c.112-4A>T	ENSP00000509223.1:n.112-4A>T
ENST00000256078.10:c.183A>T MANE Plus Clinical	ENSP00000256078.5:p.Gln61His
ENST00000311936.8:c.183A>T MANE Select	ENSP00000308495.3:p.Gln61His
ENST00000256078.8:c.183A>T	ENSP00000256078.4:p.Gln61His
ENST00000311936.7:c.183A>T	ENSP00000308495.3:p.Gln61His
ENST00000557334.5:c.112-17430A>T	ENSP00000452512.1:n.112-17430A>T
NM_004985.4:c.183A>T	NP_004976.2:p.Gln61His
NM_033360.3:c.183A>T	NP_203524.1:p.Gln61His
XM_006719069.2:c.183A>T	XP_006719132.1:p.Gln61His
XM_011520653.1:c.183A>T	XP_011518955.1:p.Gln61His
XM_006719069.4:c.183A>T	XP_006719132.1:p.Gln61His
XM_011520653.3:c.183A>T	XP_011518955.1:p.Gln61His
NM_001369786.1:c.183A>T	NP_001356715.1:p.Gln61His
NM_001369787.1:c.183A>T	NP_001356716.1:p.Gln61His
NM_004985.5:c.183A>T MANE Select	NP_004976.2:p.Gln61His
NM_033360.4:c.183A>T MANE Plus Clinical	NP_203524.1:p.Gln61His