Canonical Allele Identifier: CA368977712
Gene: MET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116755405T>A , CM000669.2:g.116755405T>A GRCh38
NC_000007.13:g.116395459T>A , CM000669.1:g.116395459T>A GRCh37
NC_000007.12:g.116182695T>A NCBI36
NG_008996.1:g.88001T>A , LRG_662:g.88001T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.1752T>A ENSP00000398776.2:p.Cys584Ter
ENST00000436117.3:c.1752T>A ENSP00000410980.2:p.Cys584Ter
ENST00000318493.11:c.1752T>A ENSP00000317272.6:p.Cys584Ter
ENST00000397752.8:c.1752T>A MANE Select ENSP00000380860.3:p.Cys584Ter
ENST00000318493.10:c.1752T>A ENSP00000317272.6:p.Cys584Ter
ENST00000397752.7:c.1752T>A ENSP00000380860.3:p.Cys584Ter
ENST00000436117.2:c.1752T>A ENSP00000410980.2:p.Cys584Ter
ENST00000495962.1:n.732T>A
NM_000245.2:c.1752T>A NP_000236.2:p.Cys584Ter
NM_001127500.1:c.1752T>A , LRG_662t1:c.1752T>A NP_001120972.1:p.Cys584Ter
XM_006715990.2:c.462T>A XP_006716053.1:p.Cys154Ter
XM_006715991.2:c.462T>A XP_006716054.1:p.Cys154Ter
XM_011516223.1:c.1809T>A XP_011514525.1:p.Cys603Ter
NM_000245.3:c.1752T>A NP_000236.2:p.Cys584Ter
NM_001127500.2:c.1752T>A NP_001120972.1:p.Cys584Ter
NM_001324401.1:c.1752T>A NP_001311330.1:p.Cys584Ter
NM_001324402.1:c.462T>A NP_001311331.1:p.Cys154Ter
XR_001744772.1:n.1983T>A
NM_001127500.3:c.1752T>A NP_001120972.1:p.Cys584Ter
NM_000245.4:c.1752T>A MANE Select NP_000236.2:p.Cys584Ter
NM_001324401.2:c.1752T>A NP_001311330.1:p.Cys584Ter
NM_001324402.2:c.462T>A NP_001311331.1:p.Cys154Ter
NM_001324401.3:c.1752T>A NP_001311330.1:p.Cys584Ter