Canonical Allele Identifier: CA2715551690
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2117039870

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116777414del , CM000669.2:g.116777414del GRCh38
NC_000007.13:g.116417468del , CM000669.1:g.116417468del GRCh37
NC_000007.12:g.116204704del NCBI36
NG_008996.1:g.110010del , LRG_662:g.110010del

Transcript Alleles

HGVS Amino-acid change
ENST00000436117.3:c.*890del ENSP00000410980.2:n.*890del
ENST00000318493.11:c.3339del ENSP00000317272.6:p.Thr1114LeufsTer14
ENST00000397752.8:c.3285del MANE Select ENSP00000380860.3:p.Thr1096LeufsTer14
ENST00000318493.10:c.3339del ENSP00000317272.6:p.Thr1114LeufsTer14
ENST00000397752.7:c.3285del ENSP00000380860.3:p.Thr1096LeufsTer14
NM_000245.2:c.3285del NP_000236.2:p.Thr1096LeufsTer14
NM_001127500.1:c.3339del , LRG_662t1:c.3339del NP_001120972.1:p.Thr1114LeufsTer14
XM_006715990.2:c.1995del XP_006716053.1:p.Thr666LeufsTer14
XM_006715991.2:c.1995del XP_006716054.1:p.Thr666LeufsTer14
XM_011516223.1:c.3342del XP_011514525.1:p.Thr1115LeufsTer14
NM_000245.3:c.3285del NP_000236.2:p.Thr1096LeufsTer14
NM_001127500.2:c.3339del NP_001120972.1:p.Thr1114LeufsTer14
NM_001324402.1:c.1995del NP_001311331.1:p.Thr666LeufsTer14
XR_001744772.1:n.3416del
NM_001127500.3:c.3339del NP_001120972.1:p.Thr1114LeufsTer14
NM_000245.4:c.3285del MANE Select NP_000236.2:p.Thr1096LeufsTer14
NM_001324402.2:c.1995del NP_001311331.1:p.Thr666LeufsTer14