Canonical Allele Identifier: CA408105069

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3671692-G-T
• MyVariant Identifiers: chr20:g.3652339G>T (hg19) ; chr20:g.3671692G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671692G>T , CM000682.2:g.3671692G>T	GRCh38
NC_000020.10:g.3652339G>T , CM000682.1:g.3652339G>T	GRCh37
NC_000020.9:g.3600339G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1794C>A MANE Select	ENSP00000348912.3:p.His598Gln
ENST00000350009.6:c.1794C>A	ENSP00000322550.5:p.His598Gln
ENST00000356518.6:c.1794C>A	ENSP00000348912.2:p.His598Gln
ENST00000379861.8:c.1794C>A	ENSP00000369190.4:p.His598Gln
ENST00000466620.5:n.1433C>A
ENST00000617732.1:c.*632-235C>A	ENSP00000483343.1:n.*632-235C>A
ENST00000619289.4:c.1434C>A	ENSP00000484600.1:p.His478Gln
NM_001282447.1:c.1794C>A	NP_001269376.1:p.His598Gln
NM_025220.3:c.1794C>A	NP_079496.1:p.His598Gln
NM_153202.2:c.1794C>A	NP_694882.1:p.His598Gln
XM_005260843.1:c.1833C>A	XP_005260900.1:p.His611Gln
XM_006723639.1:c.1833C>A	XP_006723702.1:p.His611Gln
XM_006723640.1:c.1824C>A	XP_006723703.1:p.His608Gln
XM_011529366.1:c.1830C>A	XP_011527668.1:p.His610Gln
XM_011529367.1:c.1791C>A	XP_011527669.1:p.His597Gln
XM_011529368.1:c.1833C>A	XP_011527670.1:p.His611Gln
XM_011529369.1:c.1801C>A	XP_011527671.1:p.Pro601Thr
XM_011529370.1:c.1801C>A	XP_011527672.1:p.Pro601Thr
XM_011529373.1:c.831C>A	XP_011527675.1:p.His277Gln
XR_937151.1:n.1937C>A
XR_937152.1:n.1937C>A
XR_937153.1:n.1818C>A
XR_937154.1:n.1818C>A
XR_937155.1:n.1739C>A
XR_937157.1:n.1741C>A
NM_001282447.2:c.1794C>A	NP_001269376.1:p.His598Gln
NM_025220.4:c.1794C>A	NP_079496.1:p.His598Gln
NM_153202.3:c.1794C>A	NP_694882.1:p.His598Gln
XM_011529373.2:c.831C>A	XP_011527675.1:p.His277Gln
XR_001754405.1:n.1905C>A
XR_002958534.1:n.2014C>A
NM_001282447.3:c.1794C>A	NP_001269376.1:p.His598Gln
NM_025220.5:c.1794C>A MANE Select	NP_079496.1:p.His598Gln
NM_153202.4:c.1794C>A	NP_694882.1:p.His598Gln