Canonical Allele Identifier: CA408104883

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3671596-C-A
• MyVariant Identifiers: chr20:g.3652243C>A (hg19) ; chr20:g.3671596C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671596C>A , CM000682.2:g.3671596C>A	GRCh38
NC_000020.10:g.3652243C>A , CM000682.1:g.3652243C>A	GRCh37
NC_000020.9:g.3600243C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1890G>T MANE Select	ENSP00000348912.3:p.Gln630His
ENST00000350009.6:c.1890G>T	ENSP00000322550.5:p.Gln630His
ENST00000356518.6:c.1890G>T	ENSP00000348912.2:p.Gln630His
ENST00000379861.8:c.1890G>T	ENSP00000369190.4:p.Gln630His
ENST00000466620.5:n.1529G>T
ENST00000617732.1:c.*632-139G>T	ENSP00000483343.1:n.*632-139G>T
ENST00000619289.4:c.1530G>T	ENSP00000484600.1:p.Gln510His
NM_001282447.1:c.1890G>T	NP_001269376.1:p.Gln630His
NM_025220.3:c.1890G>T	NP_079496.1:p.Gln630His
NM_153202.2:c.1890G>T	NP_694882.1:p.Gln630His
XM_005260843.1:c.1929G>T	XP_005260900.1:p.Gln643His
XM_006723639.1:c.1929G>T	XP_006723702.1:p.Gln643His
XM_006723640.1:c.1920G>T	XP_006723703.1:p.Gln640His
XM_011529366.1:c.1926G>T	XP_011527668.1:p.Gln642His
XM_011529367.1:c.1887G>T	XP_011527669.1:p.Gln629His
XM_011529368.1:c.1929G>T	XP_011527670.1:p.Gln643His
XM_011529369.1:c.1897G>T	XP_011527671.1:p.Val633Leu
XM_011529370.1:c.1897G>T	XP_011527672.1:p.Val633Leu
XM_011529373.1:c.927G>T	XP_011527675.1:p.Gln309His
XR_937151.1:n.2033G>T
XR_937152.1:n.2033G>T
XR_937153.1:n.1914G>T
XR_937154.1:n.1914G>T
XR_937155.1:n.1835G>T
XR_937157.1:n.1837G>T
NM_001282447.2:c.1890G>T	NP_001269376.1:p.Gln630His
NM_025220.4:c.1890G>T	NP_079496.1:p.Gln630His
NM_153202.3:c.1890G>T	NP_694882.1:p.Gln630His
XM_011529373.2:c.927G>T	XP_011527675.1:p.Gln309His
XR_001754405.1:n.2001G>T
XR_002958534.1:n.2110G>T
NM_001282447.3:c.1890G>T	NP_001269376.1:p.Gln630His
NM_025220.5:c.1890G>T MANE Select	NP_079496.1:p.Gln630His
NM_153202.4:c.1890G>T	NP_694882.1:p.Gln630His