Canonical Allele Identifier: CA509559922

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3671662-T-C
• MyVariant Identifiers: chr20:g.3652309T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671662T>C , CM000682.2:g.3671662T>C	GRCh38
NC_000020.10:g.3652309T>C , CM000682.1:g.3652309T>C	GRCh37
NC_000020.9:g.3600309T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1824A>G MANE Select	ENSP00000348912.3:p.Gly608=
ENST00000350009.6:c.1824A>G	ENSP00000322550.5:p.Gly608=
ENST00000356518.6:c.1824A>G	ENSP00000348912.2:p.Gly608=
ENST00000379861.8:c.1824A>G	ENSP00000369190.4:p.Gly608=
ENST00000466620.5:n.1463A>G
ENST00000617732.1:c.*632-205A>G	ENSP00000483343.1:n.*632-205A>G
ENST00000619289.4:c.1464A>G	ENSP00000484600.1:p.Gly488=
NM_001282447.1:c.1824A>G	NP_001269376.1:p.Gly608=
NM_025220.3:c.1824A>G	NP_079496.1:p.Gly608=
NM_153202.2:c.1824A>G	NP_694882.1:p.Gly608=
XM_005260843.1:c.1863A>G	XP_005260900.1:p.Gly621=
XM_006723639.1:c.1863A>G	XP_006723702.1:p.Gly621=
XM_006723640.1:c.1854A>G	XP_006723703.1:p.Gly618=
XM_011529366.1:c.1860A>G	XP_011527668.1:p.Gly620=
XM_011529367.1:c.1821A>G	XP_011527669.1:p.Gly607=
XM_011529368.1:c.1863A>G	XP_011527670.1:p.Gly621=
XM_011529369.1:c.1831A>G	XP_011527671.1:p.Ser611Gly
XM_011529370.1:c.1831A>G	XP_011527672.1:p.Ser611Gly
XM_011529373.1:c.861A>G	XP_011527675.1:p.Gly287=
XR_937151.1:n.1967A>G
XR_937152.1:n.1967A>G
XR_937153.1:n.1848A>G
XR_937154.1:n.1848A>G
XR_937155.1:n.1769A>G
XR_937157.1:n.1771A>G
NM_001282447.2:c.1824A>G	NP_001269376.1:p.Gly608=
NM_025220.4:c.1824A>G	NP_079496.1:p.Gly608=
NM_153202.3:c.1824A>G	NP_694882.1:p.Gly608=
XM_011529373.2:c.861A>G	XP_011527675.1:p.Gly287=
XR_001754405.1:n.1935A>G
XR_002958534.1:n.2044A>G
NM_001282447.3:c.1824A>G	NP_001269376.1:p.Gly608=
NM_025220.5:c.1824A>G MANE Select	NP_079496.1:p.Gly608=
NM_153202.4:c.1824A>G	NP_694882.1:p.Gly608=