Canonical Allele Identifier: CA215608
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 41608
dbSNP Id: rs200690492

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116700103A>G , CM000669.2:g.116700103A>G GRCh38
NC_000007.13:g.116340157A>G , CM000669.1:g.116340157A>G GRCh37
NC_000007.12:g.116127393A>G NCBI36
NG_008996.1:g.32699A>G , LRG_662:g.32699A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318493.11:c.1019A>G ENSP00000317272.6:p.Asp340Gly
ENST00000397752.8:c.1019A>G MANE Select ENSP00000380860.3:p.Asp340Gly
ENST00000318493.10:c.1019A>G ENSP00000317272.6:p.Asp340Gly
ENST00000397752.7:c.1019A>G ENSP00000380860.3:p.Asp340Gly
ENST00000436117.2:n.1019A>G ENSP00000410980.2:p.Asp340Gly
NM_000245.2:c.1019A>G NP_000236.2:p.Asp340Gly
NM_001127500.1:c.1019A>G , LRG_662t1:c.1019A>G NP_001120972.1:p.Asp340Gly
XM_006715991.2:c.-91+27526A>G XP_006716054.1:p.=
XM_011516223.1:c.1076A>G XP_011514525.1:p.Asp359Gly
NM_000245.3:c.1019A>G NP_000236.2:p.Asp340Gly
NM_001127500.2:c.1019A>G NP_001120972.1:p.Asp340Gly
NM_001324401.1:c.1019A>G NP_001311330.1:p.Asp340Gly
NM_001324402.1:c.-91+27526A>G NP_001311331.1:p.=
XR_001744772.1:n.1250A>G
NM_001127500.3:c.1019A>G NP_001120972.1:p.Asp340Gly
NM_000245.4:c.1019A>G MANE Select NP_000236.2:p.Asp340Gly
NM_001324401.2:c.1019A>G NP_001311330.1:p.Asp340Gly
NM_001324402.2:c.-91+27526A>G NP_001311331.1:p.=
NM_001324401.3:c.1019A>G NP_001311330.1:p.Asp340Gly