Canonical Allele Identifier: CA212644
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 183686
dbSNP Id: rs794728016

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116763206T>G , CM000669.2:g.116763206T>G GRCh38
NC_000007.13:g.116403260T>G , CM000669.1:g.116403260T>G GRCh37
NC_000007.12:g.116190496T>G NCBI36
NG_008996.1:g.95802T>G , LRG_662:g.95802T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2521T>G ENSP00000398776.2:p.Phe841Val
ENST00000436117.3:c.*126T>G ENSP00000410980.2:n.*126T>G
ENST00000318493.11:c.2575T>G ENSP00000317272.6:p.Phe859Val
ENST00000397752.8:c.2521T>G MANE Select ENSP00000380860.3:p.Phe841Val
ENST00000318493.10:c.2575T>G ENSP00000317272.6:p.Phe859Val
ENST00000397752.7:c.2521T>G ENSP00000380860.3:p.Phe841Val
ENST00000422097.1:c.361T>G ENSP00000398776.1:p.Phe121Val
NM_000245.2:c.2521T>G NP_000236.2:p.Phe841Val
NM_001127500.1:c.2575T>G , LRG_662t1:c.2575T>G NP_001120972.1:p.Phe859Val
XM_006715990.2:c.1231T>G XP_006716053.1:p.Phe411Val
XM_006715991.2:c.1231T>G XP_006716054.1:p.Phe411Val
XM_011516223.1:c.2578T>G XP_011514525.1:p.Phe860Val
NM_000245.3:c.2521T>G NP_000236.2:p.Phe841Val
NM_001127500.2:c.2575T>G NP_001120972.1:p.Phe859Val
NM_001324401.1:c.2521T>G NP_001311330.1:p.Phe841Val
NM_001324402.1:c.1231T>G NP_001311331.1:p.Phe411Val
XR_001744772.1:n.2652T>G
NM_001127500.3:c.2575T>G NP_001120972.1:p.Phe859Val
NM_000245.4:c.2521T>G MANE Select NP_000236.2:p.Phe841Val
NM_001324401.2:c.2521T>G NP_001311330.1:p.Phe841Val
NM_001324402.2:c.1231T>G NP_001311331.1:p.Phe411Val
NM_001324401.3:c.2521T>G NP_001311330.1:p.Phe841Val