Canonical Allele Identifier: CA408103787

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669579-C-T
• MyVariant Identifiers: chr20:g.3650226C>T (hg19) ; chr20:g.3669579C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669579C>T , CM000682.2:g.3669579C>T	GRCh38
NC_000020.10:g.3650226C>T , CM000682.1:g.3650226C>T	GRCh37
NC_000020.9:g.3598226C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2299G>A MANE Select	ENSP00000348912.3:p.Gly767Ser
ENST00000350009.6:c.2221G>A	ENSP00000322550.5:p.Gly741Ser
ENST00000356518.6:c.2299G>A	ENSP00000348912.2:p.Gly767Ser
ENST00000379861.8:c.2299G>A	ENSP00000369190.4:p.Gly767Ser
ENST00000466620.5:n.1860G>A
ENST00000483362.1:n.1047G>A
ENST00000617732.1:c.*986G>A	ENSP00000483343.1:n.*986G>A
ENST00000619289.4:c.1939G>A	ENSP00000484600.1:p.Gly647Ser
NM_001282447.1:c.2299G>A	NP_001269376.1:p.Gly767Ser
NM_025220.3:c.2299G>A	NP_079496.1:p.Gly767Ser
NM_153202.2:c.2221G>A	NP_694882.1:p.Gly741Ser
XM_005260843.1:c.2338G>A	XP_005260900.1:p.Gly780Ser
XM_006723639.1:c.2338G>A	XP_006723702.1:p.Gly780Ser
XM_006723640.1:c.2329G>A	XP_006723703.1:p.Gly777Ser
XM_011529366.1:c.2335G>A	XP_011527668.1:p.Gly779Ser
XM_011529367.1:c.2296G>A	XP_011527669.1:p.Gly766Ser
XM_011529368.1:c.2260G>A	XP_011527670.1:p.Gly754Ser
XM_011529373.1:c.1336G>A	XP_011527675.1:p.Gly446Ser
XR_937151.1:n.2384-209G>A
XR_937152.1:n.2384-209G>A
XR_937153.1:n.2323G>A
XR_937154.1:n.2323G>A
XR_937155.1:n.2244G>A
XR_937157.1:n.2246G>A
NM_001282447.2:c.2299G>A	NP_001269376.1:p.Gly767Ser
NM_025220.4:c.2299G>A	NP_079496.1:p.Gly767Ser
NM_153202.3:c.2221G>A	NP_694882.1:p.Gly741Ser
XM_011529373.2:c.1336G>A	XP_011527675.1:p.Gly446Ser
XR_001754405.1:n.2410G>A
XR_002958534.1:n.2519G>A
NM_001282447.3:c.2299G>A	NP_001269376.1:p.Gly767Ser
NM_025220.5:c.2299G>A MANE Select	NP_079496.1:p.Gly767Ser
NM_153202.4:c.2221G>A	NP_694882.1:p.Gly741Ser