Canonical Allele Identifier: CA2684592645
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2117064669

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783261A>T , CM000669.2:g.116783261A>T GRCh38
NC_000007.13:g.116423315A>T , CM000669.1:g.116423315A>T GRCh37
NC_000007.12:g.116210551A>T NCBI36
NG_008996.1:g.115857A>T , LRG_662:g.115857A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000436117.3:c.*1238-43A>T ENSP00000410980.2:n.*1238-43A>T
ENST00000318493.11:c.3687-43A>T ENSP00000317272.6:n.3687-43A>T
ENST00000397752.8:c.3633-43A>T MANE Select ENSP00000380860.3:n.3633-43A>T
ENST00000318493.10:c.3687-43A>T ENSP00000317272.6:n.3687-43A>T
ENST00000397752.7:c.3633-43A>T ENSP00000380860.3:n.3633-43A>T
NM_000245.2:c.3633-43A>T NP_000236.2:n.3633-43A>T
NM_001127500.1:c.3687-43A>T , LRG_662t1:c.3687-43A>T NP_001120972.1:n.3687-43A>T
XM_006715990.2:c.2343-43A>T XP_006716053.1:n.2343-43A>T
XM_006715991.2:c.2343-43A>T XP_006716054.1:n.2343-43A>T
XM_011516223.1:c.3690-43A>T XP_011514525.1:n.3690-43A>T
NM_000245.3:c.3633-43A>T NP_000236.2:n.3633-43A>T
NM_001127500.2:c.3687-43A>T NP_001120972.1:n.3687-43A>T
NM_001324402.1:c.2343-43A>T NP_001311331.1:n.2343-43A>T
XR_001744772.1:n.3764-43A>T
NM_001127500.3:c.3687-43A>T NP_001120972.1:n.3687-43A>T
NM_000245.4:c.3633-43A>T MANE Select NP_000236.2:n.3633-43A>T
NM_001324402.2:c.2343-43A>T NP_001311331.1:n.2343-43A>T