Canonical Allele Identifier: CA408103829

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669599C>T , CM000682.2:g.3669599C>T	GRCh38
NC_000020.10:g.3650246C>T , CM000682.1:g.3650246C>T	GRCh37
NC_000020.9:g.3598246C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2279G>A MANE Select	NP_079496.1:p.Gly760Asp
ENST00000356518.7:c.2279G>A MANE Select	ENSP00000348912.3:p.Gly760Asp
NM_001282447.1:c.2279G>A	NP_001269376.1:p.Gly760Asp
NM_001282447.2:c.2279G>A	NP_001269376.1:p.Gly760Asp
NM_001282447.3:c.2279G>A	NP_001269376.1:p.Gly760Asp
NM_025220.3:c.2279G>A	NP_079496.1:p.Gly760Asp
NM_025220.4:c.2279G>A	NP_079496.1:p.Gly760Asp
NM_153202.2:c.2201G>A	NP_694882.1:p.Gly734Asp
NM_153202.3:c.2201G>A	NP_694882.1:p.Gly734Asp
NM_153202.4:c.2201G>A	NP_694882.1:p.Gly734Asp
ENST00000350009.6:c.2201G>A	ENSP00000322550.5:p.Gly734Asp
ENST00000356518.6:c.2279G>A	ENSP00000348912.2:p.Gly760Asp
ENST00000379861.8:c.2279G>A	ENSP00000369190.4:p.Gly760Asp
ENST00000466620.5:n.1840G>A
ENST00000483362.1:n.1027G>A
ENST00000617732.1:c.*966G>A	ENSP00000483343.1:n.*966G>A
ENST00000619289.4:c.1919G>A	ENSP00000484600.1:p.Gly640Asp
XM_005260843.1:c.2318G>A	XP_005260900.1:p.Gly773Asp
XM_006723639.1:c.2318G>A	XP_006723702.1:p.Gly773Asp
XM_006723640.1:c.2309G>A	XP_006723703.1:p.Gly770Asp
XM_011529366.1:c.2315G>A	XP_011527668.1:p.Gly772Asp
XM_011529367.1:c.2276G>A	XP_011527669.1:p.Gly759Asp
XM_011529368.1:c.2240G>A	XP_011527670.1:p.Gly747Asp
XM_011529373.1:c.1316G>A	XP_011527675.1:p.Gly439Asp
XM_011529373.2:c.1316G>A	XP_011527675.1:p.Gly439Asp
XR_001754405.1:n.2390G>A
XR_002958534.1:n.2499G>A
XR_937151.1:n.2384-229G>A
XR_937152.1:n.2384-229G>A
XR_937153.1:n.2303G>A
XR_937154.1:n.2303G>A
XR_937155.1:n.2224G>A
XR_937157.1:n.2226G>A