Canonical Allele Identifier: CA2346677699
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669587A= , CM000682.2:g.3669587A= GRCh38
NC_000020.10:g.3650234A= , CM000682.1:g.3650234A= GRCh37
NC_000020.9:g.3598234A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2291T= MANE Select ENSP00000348912.3:p.Met764=
ENST00000350009.6:c.2213T= ENSP00000322550.5:p.Met738=
ENST00000356518.6:c.2291T= ENSP00000348912.2:p.Met764=
ENST00000379861.8:c.2291T= ENSP00000369190.4:p.Met764=
ENST00000466620.5:n.1852T=
ENST00000483362.1:n.1039T=
ENST00000617732.1:c.*978T= ENSP00000483343.1:n.*978T=
ENST00000619289.4:c.1931T= ENSP00000484600.1:p.Met644=
NM_001282447.1:c.2291T= NP_001269376.1:p.Met764=
NM_025220.3:c.2291T= NP_079496.1:p.Met764=
NM_153202.2:c.2213T= NP_694882.1:p.Met738=
XM_005260843.1:c.2330T= XP_005260900.1:p.Met777=
XM_006723639.1:c.2330T= XP_006723702.1:p.Met777=
XM_006723640.1:c.2321T= XP_006723703.1:p.Met774=
XM_011529366.1:c.2327T= XP_011527668.1:p.Met776=
XM_011529367.1:c.2288T= XP_011527669.1:p.Met763=
XM_011529368.1:c.2252T= XP_011527670.1:p.Met751=
XM_011529373.1:c.1328T= XP_011527675.1:p.Met443=
XR_937151.1:n.2384-217T=
XR_937152.1:n.2384-217T=
XR_937153.1:n.2315T=
XR_937154.1:n.2315T=
XR_937155.1:n.2236T=
XR_937157.1:n.2238T=
NM_001282447.2:c.2291T= NP_001269376.1:p.Met764=
NM_025220.4:c.2291T= NP_079496.1:p.Met764=
NM_153202.3:c.2213T= NP_694882.1:p.Met738=
XM_011529373.2:c.1328T= XP_011527675.1:p.Met443=
XR_001754405.1:n.2402T=
XR_002958534.1:n.2511T=
NM_001282447.3:c.2291T= NP_001269376.1:p.Met764=
NM_025220.5:c.2291T= MANE Select NP_079496.1:p.Met764=
NM_153202.4:c.2213T= NP_694882.1:p.Met738=