Canonical Allele Identifier: CA2346677675
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669548_3669549delinsAG , CM000682.2:g.3669548_3669549delinsAG GRCh38
NC_000020.10:g.3650195_3650196delinsAG , CM000682.1:g.3650195_3650196delinsAG GRCh37
NC_000020.9:g.3598195_3598196delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2329_2330delinsCT MANE Select ENSP00000348912.3:p.Leu777=
ENST00000350009.6:c.2251_2252delinsCT ENSP00000322550.5:p.Leu751=
ENST00000356518.6:c.2329_2330delinsCT ENSP00000348912.2:p.Leu777=
ENST00000379861.8:c.2329_2330delinsCT ENSP00000369190.4:p.Leu777=
ENST00000466620.5:n.1890_1891delinsCT
ENST00000483362.1:n.1077_1078delinsCT
ENST00000617732.1:c.*1016_*1017delinsCT ENSP00000483343.1:n.*1016_*1017delinsCT
ENST00000619289.4:c.1969_1970delinsCT ENSP00000484600.1:p.Leu657=
NM_001282447.1:c.2329_2330delinsCT NP_001269376.1:p.Leu777=
NM_025220.3:c.2329_2330delinsCT NP_079496.1:p.Leu777=
NM_153202.2:c.2251_2252delinsCT NP_694882.1:p.Leu751=
XM_005260843.1:c.2368_2369delinsCT XP_005260900.1:p.Leu790=
XM_006723639.1:c.2368_2369delinsCT XP_006723702.1:p.Leu790=
XM_006723640.1:c.2359_2360delinsCT XP_006723703.1:p.Leu787=
XM_011529366.1:c.2365_2366delinsCT XP_011527668.1:p.Leu789=
XM_011529367.1:c.2326_2327delinsCT XP_011527669.1:p.Leu776=
XM_011529368.1:c.2290_2291delinsCT XP_011527670.1:p.Leu764=
XM_011529373.1:c.1366_1367delinsCT XP_011527675.1:p.Leu456=
XR_937151.1:n.2384-179_2384-178delinsCT
XR_937152.1:n.2384-179_2384-178delinsCT
XR_937153.1:n.2353_2354delinsCT
XR_937154.1:n.2353_2354delinsCT
XR_937155.1:n.2274_2275delinsCT
XR_937157.1:n.2276_2277delinsCT
NM_001282447.2:c.2329_2330delinsCT NP_001269376.1:p.Leu777=
NM_025220.4:c.2329_2330delinsCT NP_079496.1:p.Leu777=
NM_153202.3:c.2251_2252delinsCT NP_694882.1:p.Leu751=
XM_011529373.2:c.1366_1367delinsCT XP_011527675.1:p.Leu456=
XR_001754405.1:n.2440_2441delinsCT
XR_002958534.1:n.2549_2550delinsCT
NM_001282447.3:c.2329_2330delinsCT NP_001269376.1:p.Leu777=
NM_025220.5:c.2329_2330delinsCT MANE Select NP_079496.1:p.Leu777=
NM_153202.4:c.2251_2252delinsCT NP_694882.1:p.Leu751=