Canonical Allele Identifier: CA509560104

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652417C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671770C>T , CM000682.2:g.3671770C>T	GRCh38
NC_000020.10:g.3652417C>T , CM000682.1:g.3652417C>T	GRCh37
NC_000020.9:g.3600417C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1716G>A MANE Select	ENSP00000348912.3:p.Leu572=
ENST00000350009.6:c.1716G>A	ENSP00000322550.5:p.Leu572=
ENST00000356518.6:c.1716G>A	ENSP00000348912.2:p.Leu572=
ENST00000379861.8:c.1716G>A	ENSP00000369190.4:p.Leu572=
ENST00000466620.5:n.1355G>A
ENST00000617732.1:c.*632-313G>A	ENSP00000483343.1:n.*632-313G>A
ENST00000619289.4:c.1356G>A	ENSP00000484600.1:p.Leu452=
NM_001282447.1:c.1716G>A	NP_001269376.1:p.Leu572=
NM_025220.3:c.1716G>A	NP_079496.1:p.Leu572=
NM_153202.2:c.1716G>A	NP_694882.1:p.Leu572=
XM_005260843.1:c.1755G>A	XP_005260900.1:p.Leu585=
XM_006723639.1:c.1755G>A	XP_006723702.1:p.Leu585=
XM_006723640.1:c.1746G>A	XP_006723703.1:p.Leu582=
XM_011529366.1:c.1752G>A	XP_011527668.1:p.Leu584=
XM_011529367.1:c.1713G>A	XP_011527669.1:p.Leu571=
XM_011529368.1:c.1755G>A	XP_011527670.1:p.Leu585=
XM_011529369.1:c.1723G>A	XP_011527671.1:p.Val575Met
XM_011529370.1:c.1723G>A	XP_011527672.1:p.Val575Met
XM_011529373.1:c.753G>A	XP_011527675.1:p.Leu251=
XR_937151.1:n.1859G>A
XR_937152.1:n.1859G>A
XR_937153.1:n.1740G>A
XR_937154.1:n.1740G>A
XR_937155.1:n.1661G>A
XR_937157.1:n.1663G>A
NM_001282447.2:c.1716G>A	NP_001269376.1:p.Leu572=
NM_025220.4:c.1716G>A	NP_079496.1:p.Leu572=
NM_153202.3:c.1716G>A	NP_694882.1:p.Leu572=
XM_011529373.2:c.753G>A	XP_011527675.1:p.Leu251=
XR_001754405.1:n.1827G>A
XR_002958534.1:n.1936G>A
NM_001282447.3:c.1716G>A	NP_001269376.1:p.Leu572=
NM_025220.5:c.1716G>A MANE Select	NP_079496.1:p.Leu572=
NM_153202.4:c.1716G>A	NP_694882.1:p.Leu572=