Canonical Allele Identifier: CA509419210

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669351-C-T
• MyVariant Identifiers: chr20:g.3649998C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669351C>T , CM000682.2:g.3669351C>T	GRCh38
NC_000020.10:g.3649998C>T , CM000682.1:g.3649998C>T	GRCh37
NC_000020.9:g.3597998C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2352G>A MANE Select	ENSP00000348912.3:p.Glu784=
ENST00000350009.6:c.2274G>A	ENSP00000322550.5:p.Glu758=
ENST00000356518.6:c.2352G>A	ENSP00000348912.2:p.Glu784=
ENST00000379861.8:c.2352G>A	ENSP00000369190.4:p.Glu784=
ENST00000466620.5:n.1913G>A
ENST00000483362.1:n.1275G>A
ENST00000617732.1:c.*1039G>A	ENSP00000483343.1:n.*1039G>A
ENST00000619289.4:c.1992G>A	ENSP00000484600.1:p.Glu664=
NM_001282447.1:c.2352G>A	NP_001269376.1:p.Glu784=
NM_025220.3:c.2352G>A	NP_079496.1:p.Glu784=
NM_153202.2:c.2274G>A	NP_694882.1:p.Glu758=
XM_005260843.1:c.2391G>A	XP_005260900.1:p.Glu797=
XM_006723639.1:c.2391G>A	XP_006723702.1:p.Glu797=
XM_006723640.1:c.2382G>A	XP_006723703.1:p.Glu794=
XM_011529366.1:c.2388G>A	XP_011527668.1:p.Glu796=
XM_011529367.1:c.2349G>A	XP_011527669.1:p.Glu783=
XM_011529368.1:c.2313G>A	XP_011527670.1:p.Glu771=
XM_011529373.1:c.1389G>A	XP_011527675.1:p.Glu463=
XR_937151.1:n.2403G>A
XR_937152.1:n.2403G>A
XR_937153.1:n.2376G>A
XR_937154.1:n.2376G>A
XR_937155.1:n.2297G>A
XR_937157.1:n.2299G>A
NM_001282447.2:c.2352G>A	NP_001269376.1:p.Glu784=
NM_025220.4:c.2352G>A	NP_079496.1:p.Glu784=
NM_153202.3:c.2274G>A	NP_694882.1:p.Glu758=
XM_011529373.2:c.1389G>A	XP_011527675.1:p.Glu463=
XR_001754405.1:n.2463G>A
XR_002958534.1:n.2572G>A
NM_001282447.3:c.2352G>A	NP_001269376.1:p.Glu784=
NM_025220.5:c.2352G>A MANE Select	NP_079496.1:p.Glu784=
NM_153202.4:c.2274G>A	NP_694882.1:p.Glu758=