Canonical Allele Identifier: CA2974754875
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669418_3669419del , CM000682.2:g.3669418_3669419del GRCh38
NC_000020.10:g.3650065_3650066del , CM000682.1:g.3650065_3650066del GRCh37
NC_000020.9:g.3598065_3598066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2333-49_2333-48del MANE Select ENSP00000348912.3:n.2333-49_2333-48del
ENST00000350009.6:c.2255-49_2255-48del ENSP00000322550.5:n.2255-49_2255-48del
ENST00000356518.6:c.2333-49_2333-48del ENSP00000348912.2:n.2333-49_2333-48del
ENST00000379861.8:c.2333-49_2333-48del ENSP00000369190.4:n.2333-49_2333-48del
ENST00000466620.5:n.1894-49_1894-48del
ENST00000483362.1:n.1207_1208del
ENST00000617732.1:c.*1020-49_*1020-48del ENSP00000483343.1:n.*1020-49_*1020-48del
ENST00000619289.4:c.1973-49_1973-48del ENSP00000484600.1:n.1973-49_1973-48del
NM_001282447.1:c.2333-49_2333-48del NP_001269376.1:n.2333-49_2333-48del
NM_025220.3:c.2333-49_2333-48del NP_079496.1:n.2333-49_2333-48del
NM_153202.2:c.2255-49_2255-48del NP_694882.1:n.2255-49_2255-48del
XM_005260843.1:c.2372-49_2372-48del XP_005260900.1:n.2372-49_2372-48del
XM_006723639.1:c.2372-49_2372-48del XP_006723702.1:n.2372-49_2372-48del
XM_006723640.1:c.2363-49_2363-48del XP_006723703.1:n.2363-49_2363-48del
XM_011529366.1:c.2369-49_2369-48del XP_011527668.1:n.2369-49_2369-48del
XM_011529367.1:c.2330-49_2330-48del XP_011527669.1:n.2330-49_2330-48del
XM_011529368.1:c.2294-49_2294-48del XP_011527670.1:n.2294-49_2294-48del
XM_011529373.1:c.1370-49_1370-48del XP_011527675.1:n.1370-49_1370-48del
XR_937151.1:n.2384-49_2384-48del
XR_937152.1:n.2384-49_2384-48del
XR_937153.1:n.2357-49_2357-48del
XR_937154.1:n.2357-49_2357-48del
XR_937155.1:n.2278-49_2278-48del
XR_937157.1:n.2280-49_2280-48del
NM_001282447.2:c.2333-49_2333-48del NP_001269376.1:n.2333-49_2333-48del
NM_025220.4:c.2333-49_2333-48del NP_079496.1:n.2333-49_2333-48del
NM_153202.3:c.2255-49_2255-48del NP_694882.1:n.2255-49_2255-48del
XM_011529373.2:c.1370-49_1370-48del XP_011527675.1:n.1370-49_1370-48del
XR_001754405.1:n.2444-49_2444-48del
XR_002958534.1:n.2553-49_2553-48del
NM_001282447.3:c.2333-49_2333-48del NP_001269376.1:n.2333-49_2333-48del
NM_025220.5:c.2333-49_2333-48del MANE Select NP_079496.1:n.2333-49_2333-48del
NM_153202.4:c.2255-49_2255-48del NP_694882.1:n.2255-49_2255-48del