Canonical Allele Identifier: CA2346677673
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669546C= , CM000682.2:g.3669546C= GRCh38
NC_000020.10:g.3650193C= , CM000682.1:g.3650193C= GRCh37
NC_000020.9:g.3598193C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2332G= MANE Select ENSP00000348912.3:p.Asp778=
ENST00000350009.6:c.2254G= ENSP00000322550.5:p.Asp752=
ENST00000356518.6:c.2332G= ENSP00000348912.2:p.Asp778=
ENST00000379861.8:c.2332G= ENSP00000369190.4:p.Asp778=
ENST00000466620.5:n.1893G=
ENST00000483362.1:n.1080G=
ENST00000617732.1:c.*1019G= ENSP00000483343.1:n.*1019G=
ENST00000619289.4:c.1972G= ENSP00000484600.1:p.Asp658=
NM_001282447.1:c.2332G= NP_001269376.1:p.Asp778=
NM_025220.3:c.2332G= NP_079496.1:p.Asp778=
NM_153202.2:c.2254G= NP_694882.1:p.Asp752=
XM_005260843.1:c.2371G= XP_005260900.1:p.Asp791=
XM_006723639.1:c.2371G= XP_006723702.1:p.Asp791=
XM_006723640.1:c.2362G= XP_006723703.1:p.Asp788=
XM_011529366.1:c.2368G= XP_011527668.1:p.Asp790=
XM_011529367.1:c.2329G= XP_011527669.1:p.Asp777=
XM_011529368.1:c.2293G= XP_011527670.1:p.Asp765=
XM_011529373.1:c.1369G= XP_011527675.1:p.Asp457=
XR_937151.1:n.2384-176G=
XR_937152.1:n.2384-176G=
XR_937153.1:n.2356G=
XR_937154.1:n.2356G=
XR_937155.1:n.2277G=
XR_937157.1:n.2279G=
NM_001282447.2:c.2332G= NP_001269376.1:p.Asp778=
NM_025220.4:c.2332G= NP_079496.1:p.Asp778=
NM_153202.3:c.2254G= NP_694882.1:p.Asp752=
XM_011529373.2:c.1369G= XP_011527675.1:p.Asp457=
XR_001754405.1:n.2443G=
XR_002958534.1:n.2552G=
NM_001282447.3:c.2332G= NP_001269376.1:p.Asp778=
NM_025220.5:c.2332G= MANE Select NP_079496.1:p.Asp778=
NM_153202.4:c.2254G= NP_694882.1:p.Asp752=