Canonical Allele Identifier: CA408103536
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669320C>A , CM000682.2:g.3669320C>A GRCh38
NC_000020.10:g.3649967C>A , CM000682.1:g.3649967C>A GRCh37
NC_000020.9:g.3597967C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2383G>T MANE Select ENSP00000348912.3:p.Ala795Ser
ENST00000350009.6:c.2305G>T ENSP00000322550.5:p.Ala769Ser
ENST00000356518.6:c.2383G>T ENSP00000348912.2:p.Ala795Ser
ENST00000379861.8:c.2383G>T ENSP00000369190.4:p.Ala795Ser
ENST00000466620.5:n.1944G>T
ENST00000483362.1:n.1306G>T
ENST00000617732.1:c.*1070G>T ENSP00000483343.1:n.*1070G>T
ENST00000619289.4:c.2023G>T ENSP00000484600.1:p.Ala675Ser
NM_001282447.1:c.2383G>T NP_001269376.1:p.Ala795Ser
NM_025220.3:c.2383G>T NP_079496.1:p.Ala795Ser
NM_153202.2:c.2305G>T NP_694882.1:p.Ala769Ser
XM_005260843.1:c.2422G>T XP_005260900.1:p.Ala808Ser
XM_006723639.1:c.2422G>T XP_006723702.1:p.Ala808Ser
XM_006723640.1:c.2413G>T XP_006723703.1:p.Ala805Ser
XM_011529366.1:c.2419G>T XP_011527668.1:p.Ala807Ser
XM_011529367.1:c.2380G>T XP_011527669.1:p.Ala794Ser
XM_011529368.1:c.2344G>T XP_011527670.1:p.Ala782Ser
XM_011529373.1:c.1420G>T XP_011527675.1:p.Ala474Ser
XR_937151.1:n.2434G>T
XR_937152.1:n.2434G>T
XR_937153.1:n.2407G>T
XR_937154.1:n.2407G>T
XR_937155.1:n.2328G>T
XR_937157.1:n.2330G>T
NM_001282447.2:c.2383G>T NP_001269376.1:p.Ala795Ser
NM_025220.4:c.2383G>T NP_079496.1:p.Ala795Ser
NM_153202.3:c.2305G>T NP_694882.1:p.Ala769Ser
XM_011529373.2:c.1420G>T XP_011527675.1:p.Ala474Ser
XR_001754405.1:n.2494G>T
XR_002958534.1:n.2603G>T
NM_001282447.3:c.2383G>T NP_001269376.1:p.Ala795Ser
NM_025220.5:c.2383G>T MANE Select NP_079496.1:p.Ala795Ser
NM_153202.4:c.2305G>T NP_694882.1:p.Ala769Ser