Canonical Allele Identifier: CA1737025454
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs1794311908

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116759456del , CM000669.2:g.116759456del GRCh38
NC_000007.13:g.116399510del , CM000669.1:g.116399510del GRCh37
NC_000007.12:g.116186746del NCBI36
NG_008996.1:g.92052del , LRG_662:g.92052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.2330del ENSP00000398776.2:p.Ile777LysfsTer22
ENST00000436117.3:c.2264+836del ENSP00000410980.2:n.2264+836del
ENST00000318493.11:c.2384del ENSP00000317272.6:p.Ile795LysfsTer22
ENST00000397752.8:c.2330del MANE Select ENSP00000380860.3:p.Ile777LysfsTer22
ENST00000318493.10:c.2384del ENSP00000317272.6:p.Ile795LysfsTer22
ENST00000397752.7:c.2330del ENSP00000380860.3:p.Ile777LysfsTer22
ENST00000422097.1:c.170del ENSP00000398776.1:p.Ile57LysfsTer22
ENST00000436117.2:c.2264+836del ENSP00000410980.2:n.2264+836del
NM_000245.2:c.2330del NP_000236.2:p.Ile777LysfsTer22
NM_001127500.1:c.2384del , LRG_662t1:c.2384del NP_001120972.1:p.Ile795LysfsTer22
XM_006715990.2:c.1040del XP_006716053.1:p.Ile347LysfsTer22
XM_006715991.2:c.1040del XP_006716054.1:p.Ile347LysfsTer22
XM_011516223.1:c.2387del XP_011514525.1:p.Ile796LysfsTer22
NM_000245.3:c.2330del NP_000236.2:p.Ile777LysfsTer22
NM_001127500.2:c.2384del NP_001120972.1:p.Ile795LysfsTer22
NM_001324401.1:c.2330del NP_001311330.1:p.Ile777LysfsTer22
NM_001324402.1:c.1040del NP_001311331.1:p.Ile347LysfsTer22
XR_001744772.1:n.2495+836del
NM_001127500.3:c.2384del NP_001120972.1:p.Ile795LysfsTer22
NM_000245.4:c.2330del MANE Select NP_000236.2:p.Ile777LysfsTer22
NM_001324401.2:c.2330del NP_001311330.1:p.Ile777LysfsTer22
NM_001324402.2:c.1040del NP_001311331.1:p.Ile347LysfsTer22
NM_001324401.3:c.2330del NP_001311330.1:p.Ile777LysfsTer22