Canonical Allele Identifier: CA408105317
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671904T>A , CM000682.2:g.3671904T>A GRCh38
NC_000020.10:g.3652551T>A , CM000682.1:g.3652551T>A GRCh37
NC_000020.9:g.3600551T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.1679A>T MANE Select ENSP00000348912.3:p.Glu560Val
ENST00000350009.6:c.1679A>T ENSP00000322550.5:p.Glu560Val
ENST00000356518.6:c.1679A>T ENSP00000348912.2:p.Glu560Val
ENST00000379861.8:c.1679A>T ENSP00000369190.4:p.Glu560Val
ENST00000466620.5:n.1318A>T
ENST00000617732.1:c.*632-447A>T ENSP00000483343.1:n.*632-447A>T
ENST00000619289.4:c.1319A>T ENSP00000484600.1:p.Glu440Val
NM_001282447.1:c.1679A>T NP_001269376.1:p.Glu560Val
NM_025220.3:c.1679A>T NP_079496.1:p.Glu560Val
NM_153202.2:c.1679A>T NP_694882.1:p.Glu560Val
XM_005260843.1:c.1718A>T XP_005260900.1:p.Glu573Val
XM_006723639.1:c.1718A>T XP_006723702.1:p.Glu573Val
XM_006723640.1:c.1709A>T XP_006723703.1:p.Glu570Val
XM_011529366.1:c.1715A>T XP_011527668.1:p.Glu572Val
XM_011529367.1:c.1676A>T XP_011527669.1:p.Glu559Val
XM_011529368.1:c.1718A>T XP_011527670.1:p.Glu573Val
XM_011529369.1:c.1686A>T XP_011527671.1:p.Arg562=
XM_011529370.1:c.1686A>T XP_011527672.1:p.Arg562=
XM_011529373.1:c.716A>T XP_011527675.1:p.Glu239Val
XR_937151.1:n.1822A>T
XR_937152.1:n.1822A>T
XR_937153.1:n.1703A>T
XR_937154.1:n.1703A>T
XR_937155.1:n.1624A>T
XR_937157.1:n.1626A>T
NM_001282447.2:c.1679A>T NP_001269376.1:p.Glu560Val
NM_025220.4:c.1679A>T NP_079496.1:p.Glu560Val
NM_153202.3:c.1679A>T NP_694882.1:p.Glu560Val
XM_011529373.2:c.716A>T XP_011527675.1:p.Glu239Val
XR_001754405.1:n.1790A>T
XR_002958534.1:n.1899A>T
NM_001282447.3:c.1679A>T NP_001269376.1:p.Glu560Val
NM_025220.5:c.1679A>T MANE Select NP_079496.1:p.Glu560Val
NM_153202.4:c.1679A>T NP_694882.1:p.Glu560Val