Canonical Allele Identifier: CA509559837

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652577A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671930A>C , CM000682.2:g.3671930A>C	GRCh38
NC_000020.10:g.3652577A>C , CM000682.1:g.3652577A>C	GRCh37
NC_000020.9:g.3600577A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1653T>G MANE Select	ENSP00000348912.3:p.Ala551=
ENST00000350009.6:c.1653T>G	ENSP00000322550.5:p.Ala551=
ENST00000356518.6:c.1653T>G	ENSP00000348912.2:p.Ala551=
ENST00000379861.8:c.1653T>G	ENSP00000369190.4:p.Ala551=
ENST00000466620.5:n.1292T>G
ENST00000617732.1:c.*632-473T>G	ENSP00000483343.1:n.*632-473T>G
ENST00000619289.4:c.1293T>G	ENSP00000484600.1:p.Ala431=
NM_001282447.1:c.1653T>G	NP_001269376.1:p.Ala551=
NM_025220.3:c.1653T>G	NP_079496.1:p.Ala551=
NM_153202.2:c.1653T>G	NP_694882.1:p.Ala551=
XM_005260843.1:c.1692T>G	XP_005260900.1:p.Ala564=
XM_006723639.1:c.1692T>G	XP_006723702.1:p.Ala564=
XM_006723640.1:c.1683T>G	XP_006723703.1:p.Ala561=
XM_011529366.1:c.1689T>G	XP_011527668.1:p.Ala563=
XM_011529367.1:c.1650T>G	XP_011527669.1:p.Ala550=
XM_011529368.1:c.1692T>G	XP_011527670.1:p.Ala564=
XM_011529369.1:c.1660T>G	XP_011527671.1:p.Ser554Ala
XM_011529370.1:c.1660T>G	XP_011527672.1:p.Ser554Ala
XM_011529373.1:c.690T>G	XP_011527675.1:p.Ala230=
XR_937151.1:n.1796T>G
XR_937152.1:n.1796T>G
XR_937153.1:n.1677T>G
XR_937154.1:n.1677T>G
XR_937155.1:n.1598T>G
XR_937157.1:n.1600T>G
NM_001282447.2:c.1653T>G	NP_001269376.1:p.Ala551=
NM_025220.4:c.1653T>G	NP_079496.1:p.Ala551=
NM_153202.3:c.1653T>G	NP_694882.1:p.Ala551=
XM_011529373.2:c.690T>G	XP_011527675.1:p.Ala230=
XR_001754405.1:n.1764T>G
XR_002958534.1:n.1873T>G
NM_001282447.3:c.1653T>G	NP_001269376.1:p.Ala551=
NM_025220.5:c.1653T>G MANE Select	NP_079496.1:p.Ala551=
NM_153202.4:c.1653T>G	NP_694882.1:p.Ala551=