Canonical Allele Identifier: CA2346677629
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669446G= , CM000682.2:g.3669446G= GRCh38
NC_000020.10:g.3650093G= , CM000682.1:g.3650093G= GRCh37
NC_000020.9:g.3598093G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2333-76C= MANE Select ENSP00000348912.3:n.2333-76C=
ENST00000350009.6:c.2255-76C= ENSP00000322550.5:n.2255-76C=
ENST00000356518.6:c.2333-76C= ENSP00000348912.2:n.2333-76C=
ENST00000379861.8:c.2333-76C= ENSP00000369190.4:n.2333-76C=
ENST00000466620.5:n.1894-76C=
ENST00000483362.1:n.1180C=
ENST00000617732.1:c.*1020-76C= ENSP00000483343.1:n.*1020-76C=
ENST00000619289.4:c.1973-76C= ENSP00000484600.1:n.1973-76C=
NM_001282447.1:c.2333-76C= NP_001269376.1:n.2333-76C=
NM_025220.3:c.2333-76C= NP_079496.1:n.2333-76C=
NM_153202.2:c.2255-76C= NP_694882.1:n.2255-76C=
XM_005260843.1:c.2372-76C= XP_005260900.1:n.2372-76C=
XM_006723639.1:c.2372-76C= XP_006723702.1:n.2372-76C=
XM_006723640.1:c.2363-76C= XP_006723703.1:n.2363-76C=
XM_011529366.1:c.2369-76C= XP_011527668.1:n.2369-76C=
XM_011529367.1:c.2330-76C= XP_011527669.1:n.2330-76C=
XM_011529368.1:c.2294-76C= XP_011527670.1:n.2294-76C=
XM_011529373.1:c.1370-76C= XP_011527675.1:n.1370-76C=
XR_937151.1:n.2384-76C=
XR_937152.1:n.2384-76C=
XR_937153.1:n.2357-76C=
XR_937154.1:n.2357-76C=
XR_937155.1:n.2278-76C=
XR_937157.1:n.2280-76C=
NM_001282447.2:c.2333-76C= NP_001269376.1:n.2333-76C=
NM_025220.4:c.2333-76C= NP_079496.1:n.2333-76C=
NM_153202.3:c.2255-76C= NP_694882.1:n.2255-76C=
XM_011529373.2:c.1370-76C= XP_011527675.1:n.1370-76C=
XR_001754405.1:n.2444-76C=
XR_002958534.1:n.2553-76C=
NM_001282447.3:c.2333-76C= NP_001269376.1:n.2333-76C=
NM_025220.5:c.2333-76C= MANE Select NP_079496.1:n.2333-76C=
NM_153202.4:c.2255-76C= NP_694882.1:n.2255-76C=