Canonical Allele Identifier: CA2715550327
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116910071

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116755449del , CM000669.2:g.116755449del GRCh38
NC_000007.13:g.116395503del , CM000669.1:g.116395503del GRCh37
NC_000007.12:g.116182739del NCBI36
NG_008996.1:g.88045del , LRG_662:g.88045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.1796del ENSP00000398776.2:p.Lys599ArgfsTer14
ENST00000436117.3:c.1796del ENSP00000410980.2:p.Lys599ArgfsTer14
ENST00000318493.11:c.1796del ENSP00000317272.6:p.Lys599ArgfsTer14
ENST00000397752.8:c.1796del MANE Select ENSP00000380860.3:p.Lys599ArgfsTer14
ENST00000318493.10:c.1796del ENSP00000317272.6:p.Lys599ArgfsTer14
ENST00000397752.7:c.1796del ENSP00000380860.3:p.Lys599ArgfsTer14
ENST00000436117.2:c.1796del ENSP00000410980.2:p.Lys599ArgfsTer14
NM_000245.2:c.1796del NP_000236.2:p.Lys599ArgfsTer14
NM_001127500.1:c.1796del , LRG_662t1:c.1796del NP_001120972.1:p.Lys599ArgfsTer14
XM_006715990.2:c.506del XP_006716053.1:p.Lys169ArgfsTer14
XM_006715991.2:c.506del XP_006716054.1:p.Lys169ArgfsTer14
XM_011516223.1:c.1853del XP_011514525.1:p.Lys618ArgfsTer14
NM_000245.3:c.1796del NP_000236.2:p.Lys599ArgfsTer14
NM_001127500.2:c.1796del NP_001120972.1:p.Lys599ArgfsTer14
NM_001324401.1:c.1796del NP_001311330.1:p.Lys599ArgfsTer14
NM_001324402.1:c.506del NP_001311331.1:p.Lys169ArgfsTer14
XR_001744772.1:n.2027del
NM_001127500.3:c.1796del NP_001120972.1:p.Lys599ArgfsTer14
NM_000245.4:c.1796del MANE Select NP_000236.2:p.Lys599ArgfsTer14
NM_001324401.2:c.1796del NP_001311330.1:p.Lys599ArgfsTer14
NM_001324402.2:c.506del NP_001311331.1:p.Lys169ArgfsTer14
NM_001324401.3:c.1796del NP_001311330.1:p.Lys599ArgfsTer14