Canonical Allele Identifier: CA1737025603
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116759510_116759511delinsGT , CM000669.2:g.116759510_116759511delinsGT GRCh38
NC_000007.13:g.116399564_116399565delinsGT , CM000669.1:g.116399564_116399565delinsGT GRCh37
NC_000007.12:g.116186800_116186801delinsGT NCBI36
NG_008996.1:g.92106_92107delinsGT , LRG_662:g.92106_92107delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.2364+20_2364+21delinsGT ENSP00000398776.2:n.2364+20_2364+21delinsGT
ENST00000436117.3:c.2264+890_2264+891delinsGT ENSP00000410980.2:n.2264+890_2264+891delinsGT
ENST00000318493.11:c.2418+20_2418+21delinsGT ENSP00000317272.6:n.2418+20_2418+21delinsGT
ENST00000397752.8:c.2364+20_2364+21delinsGT MANE Select ENSP00000380860.3:n.2364+20_2364+21delinsGT
ENST00000318493.10:c.2418+20_2418+21delinsGT ENSP00000317272.6:n.2418+20_2418+21delinsGT
ENST00000397752.7:c.2364+20_2364+21delinsGT ENSP00000380860.3:n.2364+20_2364+21delinsGT
ENST00000422097.1:c.204+20_204+21delinsGT ENSP00000398776.1:n.204+20_204+21delinsGT
ENST00000436117.2:c.2264+890_2264+891delinsGT ENSP00000410980.2:n.2264+890_2264+891delinsGT
NM_000245.2:c.2364+20_2364+21delinsGT NP_000236.2:n.2364+20_2364+21delinsGT
NM_001127500.1:c.2418+20_2418+21delinsGT , LRG_662t1:c.2418+20_2418+21delinsGT NP_001120972.1:n.2418+20_2418+21delinsGT
XM_006715990.2:c.1074+20_1074+21delinsGT XP_006716053.1:n.1074+20_1074+21delinsGT
XM_006715991.2:c.1074+20_1074+21delinsGT XP_006716054.1:n.1074+20_1074+21delinsGT
XM_011516223.1:c.2421+20_2421+21delinsGT XP_011514525.1:n.2421+20_2421+21delinsGT
NM_000245.3:c.2364+20_2364+21delinsGT NP_000236.2:n.2364+20_2364+21delinsGT
NM_001127500.2:c.2418+20_2418+21delinsGT NP_001120972.1:n.2418+20_2418+21delinsGT
NM_001324401.1:c.2364+20_2364+21delinsGT NP_001311330.1:n.2364+20_2364+21delinsGT
NM_001324402.1:c.1074+20_1074+21delinsGT NP_001311331.1:n.1074+20_1074+21delinsGT
XR_001744772.1:n.2495+890_2495+891delinsGT
NM_001127500.3:c.2418+20_2418+21delinsGT NP_001120972.1:n.2418+20_2418+21delinsGT
NM_000245.4:c.2364+20_2364+21delinsGT MANE Select NP_000236.2:n.2364+20_2364+21delinsGT
NM_001324401.2:c.2364+20_2364+21delinsGT NP_001311330.1:n.2364+20_2364+21delinsGT
NM_001324402.2:c.1074+20_1074+21delinsGT NP_001311331.1:n.1074+20_1074+21delinsGT
NM_001324401.3:c.2364+20_2364+21delinsGT NP_001311330.1:n.2364+20_2364+21delinsGT