Canonical Allele Identifier: CA368986780
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1470365
ClinVar RCV Id: RCV001964143
dbSNP Id: rs2116993223

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771645C>A , CM000669.2:g.116771645C>A GRCh38
NC_000007.13:g.116411699C>A , CM000669.1:g.116411699C>A GRCh37
NC_000007.12:g.116198935C>A NCBI36
NG_008996.1:g.104241C>A , LRG_662:g.104241C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*483C>A ENSP00000410980.2:n.*483C>A
ENST00000318493.11:c.2932C>A ENSP00000317272.6:p.Gln978Lys
ENST00000397752.8:c.2878C>A MANE Select ENSP00000380860.3:p.Gln960Lys
ENST00000318493.10:c.2932C>A ENSP00000317272.6:p.Gln978Lys
ENST00000397752.7:c.2878C>A ENSP00000380860.3:p.Gln960Lys
ENST00000454623.1:c.274C>A ENSP00000398140.1:p.Gln92Lys
NM_000245.2:c.2878C>A NP_000236.2:p.Gln960Lys
NM_001127500.1:c.2932C>A , LRG_662t1:c.2932C>A NP_001120972.1:p.Gln978Lys
XM_006715990.2:c.1588C>A XP_006716053.1:p.Gln530Lys
XM_006715991.2:c.1588C>A XP_006716054.1:p.Gln530Lys
XM_011516223.1:c.2935C>A XP_011514525.1:p.Gln979Lys
NM_000245.3:c.2878C>A NP_000236.2:p.Gln960Lys
NM_001127500.2:c.2932C>A NP_001120972.1:p.Gln978Lys
NM_001324402.1:c.1588C>A NP_001311331.1:p.Gln530Lys
XR_001744772.1:n.3009C>A
NM_001127500.3:c.2932C>A NP_001120972.1:p.Gln978Lys
NM_000245.4:c.2878C>A MANE Select NP_000236.2:p.Gln960Lys
NM_001324402.2:c.1588C>A NP_001311331.1:p.Gln530Lys