Canonical Allele Identifier: CA279964
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12595
ClinVar RCV Id: RCV000013426 RCV000157942 RCV001205658 RCV003390676
dbSNP Id: rs104894362
COSMIC: COSM5347094
MyVariant Identifiers: chr12:g.25362828G>C (hg19) chr12:g.25209894G>C (hg38)
PubMed: PMID:17056636 PMID:18386799
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209894G>C , CM000674.2:g.25209894G>C GRCh38
NC_000012.11:g.25362828G>C , CM000674.1:g.25362828G>C GRCh37
NC_000012.10:g.25254095G>C NCBI36
NG_007524.1:g.46027C>G
NG_007524.2:g.46110C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.129C>G ENSP00000452512.1:p.Phe43Leu
ENST00000685328.1:c.468C>G ENSP00000508921.1:p.Phe156Leu
ENST00000686877.1:c.*439C>G ENSP00000510431.1:n.*439C>G
ENST00000687356.1:c.*166C>G ENSP00000510511.1:n.*166C>G
ENST00000688228.1:n.942C>G
ENST00000688940.1:c.468C>G ENSP00000509238.1:p.Phe156Leu
ENST00000690406.1:c.271C>G
ENST00000690804.1:c.*429C>G ENSP00000508568.1:n.*429C>G
ENST00000692768.1:c.270C>G ENSP00000510254.1:p.Phe90Leu
ENST00000693229.1:c.393C>G ENSP00000509223.1:p.Phe131Leu
ENST00000256078.10:c.*22C>G MANE Plus Clinical ENSP00000256078.5:n.*22C>G
ENST00000311936.8:c.468C>G MANE Select ENSP00000308495.3:p.Phe156Leu
ENST00000256078.8:c.*22C>G ENSP00000256078.4:n.*22C>G
ENST00000311936.7:c.468C>G ENSP00000308495.3:p.Phe156Leu
ENST00000557334.5:c.129C>G ENSP00000452512.1:p.Phe43Leu
NM_004985.4:c.468C>G NP_004976.2:p.Phe156Leu
NM_033360.3:c.*22C>G NP_203524.1:n.*22C>G
XM_006719069.2:c.*22C>G XP_006719132.1:n.*22C>G
XM_011520653.1:c.468C>G XP_011518955.1:p.Phe156Leu
XM_006719069.4:c.*22C>G XP_006719132.1:n.*22C>G
XM_011520653.3:c.468C>G XP_011518955.1:p.Phe156Leu
NM_001369786.1:c.*22C>G NP_001356715.1:n.*22C>G
NM_001369787.1:c.468C>G NP_001356716.1:p.Phe156Leu
NM_004985.5:c.468C>G MANE Select NP_004976.2:p.Phe156Leu
NM_033360.4:c.*22C>G MANE Plus Clinical NP_203524.1:n.*22C>G
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