Canonical Allele Identifier: CA408105353

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652567A>C (hg19) ; chr20:g.3671920A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671920A>C , CM000682.2:g.3671920A>C	GRCh38
NC_000020.10:g.3652567A>C , CM000682.1:g.3652567A>C	GRCh37
NC_000020.9:g.3600567A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1663T>G MANE Select	ENSP00000348912.3:p.Cys555Gly
ENST00000350009.6:c.1663T>G	ENSP00000322550.5:p.Cys555Gly
ENST00000356518.6:c.1663T>G	ENSP00000348912.2:p.Cys555Gly
ENST00000379861.8:c.1663T>G	ENSP00000369190.4:p.Cys555Gly
ENST00000466620.5:n.1302T>G
ENST00000617732.1:c.*632-463T>G	ENSP00000483343.1:n.*632-463T>G
ENST00000619289.4:c.1303T>G	ENSP00000484600.1:p.Cys435Gly
NM_001282447.1:c.1663T>G	NP_001269376.1:p.Cys555Gly
NM_025220.3:c.1663T>G	NP_079496.1:p.Cys555Gly
NM_153202.2:c.1663T>G	NP_694882.1:p.Cys555Gly
XM_005260843.1:c.1702T>G	XP_005260900.1:p.Cys568Gly
XM_006723639.1:c.1702T>G	XP_006723702.1:p.Cys568Gly
XM_006723640.1:c.1693T>G	XP_006723703.1:p.Cys565Gly
XM_011529366.1:c.1699T>G	XP_011527668.1:p.Cys567Gly
XM_011529367.1:c.1660T>G	XP_011527669.1:p.Cys554Gly
XM_011529368.1:c.1702T>G	XP_011527670.1:p.Cys568Gly
XM_011529369.1:c.1670T>G	XP_011527671.1:p.Leu557Arg
XM_011529370.1:c.1670T>G	XP_011527672.1:p.Leu557Arg
XM_011529373.1:c.700T>G	XP_011527675.1:p.Cys234Gly
XR_937151.1:n.1806T>G
XR_937152.1:n.1806T>G
XR_937153.1:n.1687T>G
XR_937154.1:n.1687T>G
XR_937155.1:n.1608T>G
XR_937157.1:n.1610T>G
NM_001282447.2:c.1663T>G	NP_001269376.1:p.Cys555Gly
NM_025220.4:c.1663T>G	NP_079496.1:p.Cys555Gly
NM_153202.3:c.1663T>G	NP_694882.1:p.Cys555Gly
XM_011529373.2:c.700T>G	XP_011527675.1:p.Cys234Gly
XR_001754405.1:n.1774T>G
XR_002958534.1:n.1883T>G
NM_001282447.3:c.1663T>G	NP_001269376.1:p.Cys555Gly
NM_025220.5:c.1663T>G MANE Select	NP_079496.1:p.Cys555Gly
NM_153202.4:c.1663T>G	NP_694882.1:p.Cys555Gly