Canonical Allele Identifier: CA4448620
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411908
dbSNP Id: rs774433287

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771935A>G , CM000669.2:g.116771935A>G GRCh38
NC_000007.13:g.116411989A>G , CM000669.1:g.116411989A>G GRCh37
NC_000007.12:g.116199225A>G NCBI36
NG_008996.1:g.104531A>G , LRG_662:g.104531A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*579A>G ENSP00000410980.2:n.*579A>G
ENST00000318493.11:c.3028A>G ENSP00000317272.6:p.Thr1010Ala
ENST00000397752.8:c.2974A>G MANE Select ENSP00000380860.3:p.Thr992Ala
ENST00000318493.10:c.3028A>G ENSP00000317272.6:p.Thr1010Ala
ENST00000397752.7:c.2974A>G ENSP00000380860.3:p.Thr992Ala
ENST00000454623.1:c.283+281A>G ENSP00000398140.1:n.283+281A>G
NM_000245.2:c.2974A>G NP_000236.2:p.Thr992Ala
NM_001127500.1:c.3028A>G , LRG_662t1:c.3028A>G NP_001120972.1:p.Thr1010Ala
XM_006715990.2:c.1684A>G XP_006716053.1:p.Thr562Ala
XM_006715991.2:c.1684A>G XP_006716054.1:p.Thr562Ala
XM_011516223.1:c.3031A>G XP_011514525.1:p.Thr1011Ala
NM_000245.3:c.2974A>G NP_000236.2:p.Thr992Ala
NM_001127500.2:c.3028A>G NP_001120972.1:p.Thr1010Ala
NM_001324402.1:c.1684A>G NP_001311331.1:p.Thr562Ala
XR_001744772.1:n.3105A>G
NM_001127500.3:c.3028A>G NP_001120972.1:p.Thr1010Ala
NM_000245.4:c.2974A>G MANE Select NP_000236.2:p.Thr992Ala
NM_001324402.2:c.1684A>G NP_001311331.1:p.Thr562Ala