Canonical Allele Identifier: CA2346677681
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669558G= , CM000682.2:g.3669558G= GRCh38
NC_000020.10:g.3650205G= , CM000682.1:g.3650205G= GRCh37
NC_000020.9:g.3598205G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2320C= MANE Select ENSP00000348912.3:p.Pro774=
ENST00000350009.6:c.2242C= ENSP00000322550.5:p.Pro748=
ENST00000356518.6:c.2320C= ENSP00000348912.2:p.Pro774=
ENST00000379861.8:c.2320C= ENSP00000369190.4:p.Pro774=
ENST00000466620.5:n.1881C=
ENST00000483362.1:n.1068C=
ENST00000617732.1:c.*1007C= ENSP00000483343.1:n.*1007C=
ENST00000619289.4:c.1960C= ENSP00000484600.1:p.Pro654=
NM_001282447.1:c.2320C= NP_001269376.1:p.Pro774=
NM_025220.3:c.2320C= NP_079496.1:p.Pro774=
NM_153202.2:c.2242C= NP_694882.1:p.Pro748=
XM_005260843.1:c.2359C= XP_005260900.1:p.Pro787=
XM_006723639.1:c.2359C= XP_006723702.1:p.Pro787=
XM_006723640.1:c.2350C= XP_006723703.1:p.Pro784=
XM_011529366.1:c.2356C= XP_011527668.1:p.Pro786=
XM_011529367.1:c.2317C= XP_011527669.1:p.Pro773=
XM_011529368.1:c.2281C= XP_011527670.1:p.Pro761=
XM_011529373.1:c.1357C= XP_011527675.1:p.Pro453=
XR_937151.1:n.2384-188C=
XR_937152.1:n.2384-188C=
XR_937153.1:n.2344C=
XR_937154.1:n.2344C=
XR_937155.1:n.2265C=
XR_937157.1:n.2267C=
NM_001282447.2:c.2320C= NP_001269376.1:p.Pro774=
NM_025220.4:c.2320C= NP_079496.1:p.Pro774=
NM_153202.3:c.2242C= NP_694882.1:p.Pro748=
XM_011529373.2:c.1357C= XP_011527675.1:p.Pro453=
XR_001754405.1:n.2431C=
XR_002958534.1:n.2540C=
NM_001282447.3:c.2320C= NP_001269376.1:p.Pro774=
NM_025220.5:c.2320C= MANE Select NP_079496.1:p.Pro774=
NM_153202.4:c.2242C= NP_694882.1:p.Pro748=