Canonical Allele Identifier: CA509419183

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669312-C-A
• MyVariant Identifiers: chr20:g.3649959C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669312C>A , CM000682.2:g.3669312C>A	GRCh38
NC_000020.10:g.3649959C>A , CM000682.1:g.3649959C>A	GRCh37
NC_000020.9:g.3597959C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2391G>T MANE Select	ENSP00000348912.3:p.Ser797=
ENST00000350009.6:c.2313G>T	ENSP00000322550.5:p.Ser771=
ENST00000356518.6:c.2391G>T	ENSP00000348912.2:p.Ser797=
ENST00000379861.8:c.2391G>T	ENSP00000369190.4:p.Ser797=
ENST00000466620.5:n.1952G>T
ENST00000483362.1:n.1314G>T
ENST00000617732.1:c.*1078G>T	ENSP00000483343.1:n.*1078G>T
ENST00000619289.4:c.2031G>T	ENSP00000484600.1:p.Ser677=
NM_001282447.1:c.2391G>T	NP_001269376.1:p.Ser797=
NM_025220.3:c.2391G>T	NP_079496.1:p.Ser797=
NM_153202.2:c.2313G>T	NP_694882.1:p.Ser771=
XM_005260843.1:c.2430G>T	XP_005260900.1:p.Ser810=
XM_006723639.1:c.2430G>T	XP_006723702.1:p.Ser810=
XM_006723640.1:c.2421G>T	XP_006723703.1:p.Ser807=
XM_011529366.1:c.2427G>T	XP_011527668.1:p.Ser809=
XM_011529367.1:c.2388G>T	XP_011527669.1:p.Ser796=
XM_011529368.1:c.2352G>T	XP_011527670.1:p.Ser784=
XM_011529373.1:c.1428G>T	XP_011527675.1:p.Ser476=
XR_937151.1:n.2442G>T
XR_937152.1:n.2442G>T
XR_937153.1:n.2415G>T
XR_937154.1:n.2415G>T
XR_937155.1:n.2336G>T
XR_937157.1:n.2338G>T
NM_001282447.2:c.2391G>T	NP_001269376.1:p.Ser797=
NM_025220.4:c.2391G>T	NP_079496.1:p.Ser797=
NM_153202.3:c.2313G>T	NP_694882.1:p.Ser771=
XM_011529373.2:c.1428G>T	XP_011527675.1:p.Ser476=
XR_001754405.1:n.2502G>T
XR_002958534.1:n.2611G>T
NM_001282447.3:c.2391G>T	NP_001269376.1:p.Ser797=
NM_025220.5:c.2391G>T MANE Select	NP_079496.1:p.Ser797=
NM_153202.4:c.2313G>T	NP_694882.1:p.Ser771=