Canonical Allele Identifier: CA2974755039
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669597dup , CM000682.2:g.3669597dup GRCh38
NC_000020.10:g.3650244dup , CM000682.1:g.3650244dup GRCh37
NC_000020.9:g.3598244dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2281dup MANE Select ENSP00000348912.3:p.Val761GlyfsTer20
ENST00000350009.6:c.2203dup ENSP00000322550.5:p.Val735GlyfsTer20
ENST00000356518.6:c.2281dup ENSP00000348912.2:p.Val761GlyfsTer20
ENST00000379861.8:c.2281dup ENSP00000369190.4:p.Val761GlyfsTer20
ENST00000466620.5:n.1842dup
ENST00000483362.1:n.1029dup
ENST00000617732.1:c.*968dup ENSP00000483343.1:n.*968dup
ENST00000619289.4:c.1921dup ENSP00000484600.1:p.Val641GlyfsTer20
NM_001282447.1:c.2281dup NP_001269376.1:p.Val761GlyfsTer20
NM_025220.3:c.2281dup NP_079496.1:p.Val761GlyfsTer20
NM_153202.2:c.2203dup NP_694882.1:p.Val735GlyfsTer20
XM_005260843.1:c.2320dup XP_005260900.1:p.Val774GlyfsTer20
XM_006723639.1:c.2320dup XP_006723702.1:p.Val774GlyfsTer20
XM_006723640.1:c.2311dup XP_006723703.1:p.Val771GlyfsTer20
XM_011529366.1:c.2317dup XP_011527668.1:p.Val773GlyfsTer20
XM_011529367.1:c.2278dup XP_011527669.1:p.Val760GlyfsTer20
XM_011529368.1:c.2242dup XP_011527670.1:p.Val748GlyfsTer20
XM_011529373.1:c.1318dup XP_011527675.1:p.Val440GlyfsTer20
XR_937151.1:n.2384-227dup
XR_937152.1:n.2384-227dup
XR_937153.1:n.2305dup
XR_937154.1:n.2305dup
XR_937155.1:n.2226dup
XR_937157.1:n.2228dup
NM_001282447.2:c.2281dup NP_001269376.1:p.Val761GlyfsTer20
NM_025220.4:c.2281dup NP_079496.1:p.Val761GlyfsTer20
NM_153202.3:c.2203dup NP_694882.1:p.Val735GlyfsTer20
XM_011529373.2:c.1318dup XP_011527675.1:p.Val440GlyfsTer20
XR_001754405.1:n.2392dup
XR_002958534.1:n.2501dup
NM_001282447.3:c.2281dup NP_001269376.1:p.Val761GlyfsTer20
NM_025220.5:c.2281dup MANE Select NP_079496.1:p.Val761GlyfsTer20
NM_153202.4:c.2203dup NP_694882.1:p.Val735GlyfsTer20