Canonical Allele Identifier: CA2346677453
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669071C= , CM000682.2:g.3669071C= GRCh38
NC_000020.10:g.3649718C= , CM000682.1:g.3649718C= GRCh37
NC_000020.9:g.3597718C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2405-71G= MANE Select ENSP00000348912.3:n.2405-71G=
ENST00000350009.6:c.2327-71G= ENSP00000322550.5:n.2327-71G=
ENST00000356518.6:c.2405-71G= ENSP00000348912.2:n.2405-71G=
ENST00000379861.8:c.2405-74G= ENSP00000369190.4:n.2405-74G=
ENST00000466620.5:n.1966-71G=
ENST00000483362.1:n.1328-71G=
ENST00000617732.1:c.*1092-74G= ENSP00000483343.1:n.*1092-74G=
ENST00000619289.4:c.2045-74G= ENSP00000484600.1:n.2045-74G=
NM_001282447.1:c.2405-74G= NP_001269376.1:n.2405-74G=
NM_025220.3:c.2405-71G= NP_079496.1:n.2405-71G=
NM_153202.2:c.2327-71G= NP_694882.1:n.2327-71G=
XM_005260843.1:c.2444-71G= XP_005260900.1:n.2444-71G=
XM_006723639.1:c.2444-74G= XP_006723702.1:n.2444-74G=
XM_006723640.1:c.2435-71G= XP_006723703.1:n.2435-71G=
XM_011529366.1:c.2441-71G= XP_011527668.1:n.2441-71G=
XM_011529367.1:c.2402-71G= XP_011527669.1:n.2402-71G=
XM_011529368.1:c.2366-71G= XP_011527670.1:n.2366-71G=
XM_011529373.1:c.1442-71G= XP_011527675.1:n.1442-71G=
XR_937151.1:n.2456-71G=
XR_937152.1:n.2456-74G=
XR_937153.1:n.2429-74G=
XR_937154.1:n.2429-74G=
XR_937155.1:n.2350-74G=
XR_937157.1:n.2352-74G=
NM_001282447.2:c.2405-74G= NP_001269376.1:n.2405-74G=
NM_025220.4:c.2405-71G= NP_079496.1:n.2405-71G=
NM_153202.3:c.2327-71G= NP_694882.1:n.2327-71G=
XM_011529373.2:c.1442-71G= XP_011527675.1:n.1442-71G=
XR_001754405.1:n.2516-74G=
XR_002958534.1:n.2625-74G=
NM_001282447.3:c.2405-74G= NP_001269376.1:n.2405-74G=
NM_025220.5:c.2405-71G= MANE Select NP_079496.1:n.2405-71G=
NM_153202.4:c.2327-71G= NP_694882.1:n.2327-71G=