Canonical Allele Identifier: CA408105078

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652343A>T (hg19) ; chr20:g.3671696A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671696A>T , CM000682.2:g.3671696A>T	GRCh38
NC_000020.10:g.3652343A>T , CM000682.1:g.3652343A>T	GRCh37
NC_000020.9:g.3600343A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1790T>A MANE Select	ENSP00000348912.3:p.Val597Asp
ENST00000350009.6:c.1790T>A	ENSP00000322550.5:p.Val597Asp
ENST00000356518.6:c.1790T>A	ENSP00000348912.2:p.Val597Asp
ENST00000379861.8:c.1790T>A	ENSP00000369190.4:p.Val597Asp
ENST00000466620.5:n.1429T>A
ENST00000617732.1:c.*632-239T>A	ENSP00000483343.1:n.*632-239T>A
ENST00000619289.4:c.1430T>A	ENSP00000484600.1:p.Val477Asp
NM_001282447.1:c.1790T>A	NP_001269376.1:p.Val597Asp
NM_025220.3:c.1790T>A	NP_079496.1:p.Val597Asp
NM_153202.2:c.1790T>A	NP_694882.1:p.Val597Asp
XM_005260843.1:c.1829T>A	XP_005260900.1:p.Val610Asp
XM_006723639.1:c.1829T>A	XP_006723702.1:p.Val610Asp
XM_006723640.1:c.1820T>A	XP_006723703.1:p.Val607Asp
XM_011529366.1:c.1826T>A	XP_011527668.1:p.Val609Asp
XM_011529367.1:c.1787T>A	XP_011527669.1:p.Val596Asp
XM_011529368.1:c.1829T>A	XP_011527670.1:p.Val610Asp
XM_011529369.1:c.1797T>A	XP_011527671.1:p.Arg599=
XM_011529370.1:c.1797T>A	XP_011527672.1:p.Arg599=
XM_011529373.1:c.827T>A	XP_011527675.1:p.Val276Asp
XR_937151.1:n.1933T>A
XR_937152.1:n.1933T>A
XR_937153.1:n.1814T>A
XR_937154.1:n.1814T>A
XR_937155.1:n.1735T>A
XR_937157.1:n.1737T>A
NM_001282447.2:c.1790T>A	NP_001269376.1:p.Val597Asp
NM_025220.4:c.1790T>A	NP_079496.1:p.Val597Asp
NM_153202.3:c.1790T>A	NP_694882.1:p.Val597Asp
XM_011529373.2:c.827T>A	XP_011527675.1:p.Val276Asp
XR_001754405.1:n.1901T>A
XR_002958534.1:n.2010T>A
NM_001282447.3:c.1790T>A	NP_001269376.1:p.Val597Asp
NM_025220.5:c.1790T>A MANE Select	NP_079496.1:p.Val597Asp
NM_153202.4:c.1790T>A	NP_694882.1:p.Val597Asp