Canonical Allele Identifier: CA408105384

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652580A>T (hg19) ; chr20:g.3671933A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671933A>T , CM000682.2:g.3671933A>T	GRCh38
NC_000020.10:g.3652580A>T , CM000682.1:g.3652580A>T	GRCh37
NC_000020.9:g.3600580A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1650T>A MANE Select	ENSP00000348912.3:p.Asp550Glu
ENST00000350009.6:c.1650T>A	ENSP00000322550.5:p.Asp550Glu
ENST00000356518.6:c.1650T>A	ENSP00000348912.2:p.Asp550Glu
ENST00000379861.8:c.1650T>A	ENSP00000369190.4:p.Asp550Glu
ENST00000466620.5:n.1289T>A
ENST00000617732.1:c.*632-476T>A	ENSP00000483343.1:n.*632-476T>A
ENST00000619289.4:c.1290T>A	ENSP00000484600.1:p.Asp430Glu
NM_001282447.1:c.1650T>A	NP_001269376.1:p.Asp550Glu
NM_025220.3:c.1650T>A	NP_079496.1:p.Asp550Glu
NM_153202.2:c.1650T>A	NP_694882.1:p.Asp550Glu
XM_005260843.1:c.1689T>A	XP_005260900.1:p.Asp563Glu
XM_006723639.1:c.1689T>A	XP_006723702.1:p.Asp563Glu
XM_006723640.1:c.1680T>A	XP_006723703.1:p.Asp560Glu
XM_011529366.1:c.1686T>A	XP_011527668.1:p.Asp562Glu
XM_011529367.1:c.1647T>A	XP_011527669.1:p.Asp549Glu
XM_011529368.1:c.1689T>A	XP_011527670.1:p.Asp563Glu
XM_011529369.1:c.1657T>A	XP_011527671.1:p.Cys553Ser
XM_011529370.1:c.1657T>A	XP_011527672.1:p.Cys553Ser
XM_011529373.1:c.687T>A	XP_011527675.1:p.Asp229Glu
XR_937151.1:n.1793T>A
XR_937152.1:n.1793T>A
XR_937153.1:n.1674T>A
XR_937154.1:n.1674T>A
XR_937155.1:n.1595T>A
XR_937157.1:n.1597T>A
NM_001282447.2:c.1650T>A	NP_001269376.1:p.Asp550Glu
NM_025220.4:c.1650T>A	NP_079496.1:p.Asp550Glu
NM_153202.3:c.1650T>A	NP_694882.1:p.Asp550Glu
XM_011529373.2:c.687T>A	XP_011527675.1:p.Asp229Glu
XR_001754405.1:n.1761T>A
XR_002958534.1:n.1870T>A
NM_001282447.3:c.1650T>A	NP_001269376.1:p.Asp550Glu
NM_025220.5:c.1650T>A MANE Select	NP_079496.1:p.Asp550Glu
NM_153202.4:c.1650T>A	NP_694882.1:p.Asp550Glu