Canonical Allele Identifier: CA192400
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 185606
dbSNP Id: rs786202310

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116700165G>T , CM000669.2:g.116700165G>T GRCh38
NC_000007.13:g.116340219G>T , CM000669.1:g.116340219G>T GRCh37
NC_000007.12:g.116127455G>T NCBI36
NG_008996.1:g.32761G>T , LRG_662:g.32761G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.1081G>T ENSP00000398776.2:p.Ala361Ser
ENST00000436117.3:c.1081G>T ENSP00000410980.2:p.Ala361Ser
ENST00000318493.11:c.1081G>T ENSP00000317272.6:p.Ala361Ser
ENST00000397752.8:c.1081G>T MANE Select ENSP00000380860.3:p.Ala361Ser
ENST00000318493.10:c.1081G>T ENSP00000317272.6:p.Ala361Ser
ENST00000397752.7:c.1081G>T ENSP00000380860.3:p.Ala361Ser
ENST00000436117.2:c.1081G>T ENSP00000410980.2:p.Ala361Ser
NM_000245.2:c.1081G>T NP_000236.2:p.Ala361Ser
NM_001127500.1:c.1081G>T , LRG_662t1:c.1081G>T NP_001120972.1:p.Ala361Ser
XM_006715991.2:c.-91+27588G>T XP_006716054.1:n.-91+27588G>T
XM_011516223.1:c.1138G>T XP_011514525.1:p.Ala380Ser
NM_000245.3:c.1081G>T NP_000236.2:p.Ala361Ser
NM_001127500.2:c.1081G>T NP_001120972.1:p.Ala361Ser
NM_001324401.1:c.1081G>T NP_001311330.1:p.Ala361Ser
NM_001324402.1:c.-91+27588G>T NP_001311331.1:n.-91+27588G>T
XR_001744772.1:n.1312G>T
NM_001127500.3:c.1081G>T NP_001120972.1:p.Ala361Ser
NM_000245.4:c.1081G>T MANE Select NP_000236.2:p.Ala361Ser
NM_001324401.2:c.1081G>T NP_001311330.1:p.Ala361Ser
NM_001324402.2:c.-91+27588G>T NP_001311331.1:n.-91+27588G>T
NM_001324401.3:c.1081G>T NP_001311330.1:p.Ala361Ser