Canonical Allele Identifier: CA368991673
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2117066346

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783378G>A , CM000669.2:g.116783378G>A GRCh38
NC_000007.13:g.116423432G>A , CM000669.1:g.116423432G>A GRCh37
NC_000007.12:g.116210668G>A NCBI36
NG_008996.1:g.115974G>A , LRG_662:g.115974G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000436117.3:c.*1312G>A ENSP00000410980.2:n.*1312G>A
ENST00000318493.11:c.3761G>A ENSP00000317272.6:p.Ser1254Asn
ENST00000397752.8:c.3707G>A MANE Select ENSP00000380860.3:p.Ser1236Asn
ENST00000318493.10:c.3761G>A ENSP00000317272.6:p.Ser1254Asn
ENST00000397752.7:c.3707G>A ENSP00000380860.3:p.Ser1236Asn
NM_000245.2:c.3707G>A NP_000236.2:p.Ser1236Asn
NM_001127500.1:c.3761G>A , LRG_662t1:c.3761G>A NP_001120972.1:p.Ser1254Asn
XM_006715990.2:c.2417G>A XP_006716053.1:p.Ser806Asn
XM_006715991.2:c.2417G>A XP_006716054.1:p.Ser806Asn
XM_011516223.1:c.3764G>A XP_011514525.1:p.Ser1255Asn
NM_000245.3:c.3707G>A NP_000236.2:p.Ser1236Asn
NM_001127500.2:c.3761G>A NP_001120972.1:p.Ser1254Asn
NM_001324402.1:c.2417G>A NP_001311331.1:p.Ser806Asn
XR_001744772.1:n.3838G>A
NM_001127500.3:c.3761G>A NP_001120972.1:p.Ser1254Asn
NM_000245.4:c.3707G>A MANE Select NP_000236.2:p.Ser1236Asn
NM_001324402.2:c.2417G>A NP_001311331.1:p.Ser806Asn