Canonical Allele Identifier: CA509560043

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3671722-C-A
• MyVariant Identifiers: chr20:g.3652369C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671722C>A , CM000682.2:g.3671722C>A	GRCh38
NC_000020.10:g.3652369C>A , CM000682.1:g.3652369C>A	GRCh37
NC_000020.9:g.3600369C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1764G>T MANE Select	ENSP00000348912.3:p.Pro588=
ENST00000350009.6:c.1764G>T	ENSP00000322550.5:p.Pro588=
ENST00000356518.6:c.1764G>T	ENSP00000348912.2:p.Pro588=
ENST00000379861.8:c.1764G>T	ENSP00000369190.4:p.Pro588=
ENST00000466620.5:n.1403G>T
ENST00000617732.1:c.*632-265G>T	ENSP00000483343.1:n.*632-265G>T
ENST00000619289.4:c.1404G>T	ENSP00000484600.1:p.Pro468=
NM_001282447.1:c.1764G>T	NP_001269376.1:p.Pro588=
NM_025220.3:c.1764G>T	NP_079496.1:p.Pro588=
NM_153202.2:c.1764G>T	NP_694882.1:p.Pro588=
XM_005260843.1:c.1803G>T	XP_005260900.1:p.Pro601=
XM_006723639.1:c.1803G>T	XP_006723702.1:p.Pro601=
XM_006723640.1:c.1794G>T	XP_006723703.1:p.Pro598=
XM_011529366.1:c.1800G>T	XP_011527668.1:p.Pro600=
XM_011529367.1:c.1761G>T	XP_011527669.1:p.Pro587=
XM_011529368.1:c.1803G>T	XP_011527670.1:p.Pro601=
XM_011529369.1:c.1771G>T	XP_011527671.1:p.Ala591Ser
XM_011529370.1:c.1771G>T	XP_011527672.1:p.Ala591Ser
XM_011529373.1:c.801G>T	XP_011527675.1:p.Pro267=
XR_937151.1:n.1907G>T
XR_937152.1:n.1907G>T
XR_937153.1:n.1788G>T
XR_937154.1:n.1788G>T
XR_937155.1:n.1709G>T
XR_937157.1:n.1711G>T
NM_001282447.2:c.1764G>T	NP_001269376.1:p.Pro588=
NM_025220.4:c.1764G>T	NP_079496.1:p.Pro588=
NM_153202.3:c.1764G>T	NP_694882.1:p.Pro588=
XM_011529373.2:c.801G>T	XP_011527675.1:p.Pro267=
XR_001754405.1:n.1875G>T
XR_002958534.1:n.1984G>T
NM_001282447.3:c.1764G>T	NP_001269376.1:p.Pro588=
NM_025220.5:c.1764G>T MANE Select	NP_079496.1:p.Pro588=
NM_153202.4:c.1764G>T	NP_694882.1:p.Pro588=