Canonical Allele Identifier: CA2346678759

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671610C= , CM000682.2:g.3671610C=	GRCh38
NC_000020.10:g.3652257C= , CM000682.1:g.3652257C=	GRCh37
NC_000020.9:g.3600257C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1876G= MANE Select	ENSP00000348912.3:p.Glu626=
ENST00000350009.6:c.1876G=	ENSP00000322550.5:p.Glu626=
ENST00000356518.6:c.1876G=	ENSP00000348912.2:p.Glu626=
ENST00000379861.8:c.1876G=	ENSP00000369190.4:p.Glu626=
ENST00000466620.5:n.1515G=
ENST00000617732.1:c.*632-153G=	ENSP00000483343.1:n.*632-153G=
ENST00000619289.4:c.1516G=	ENSP00000484600.1:p.Glu506=
NM_001282447.1:c.1876G=	NP_001269376.1:p.Glu626=
NM_025220.3:c.1876G=	NP_079496.1:p.Glu626=
NM_153202.2:c.1876G=	NP_694882.1:p.Glu626=
XM_005260843.1:c.1915G=	XP_005260900.1:p.Glu639=
XM_006723639.1:c.1915G=	XP_006723702.1:p.Glu639=
XM_006723640.1:c.1906G=	XP_006723703.1:p.Glu636=
XM_011529366.1:c.1912G=	XP_011527668.1:p.Glu638=
XM_011529367.1:c.1873G=	XP_011527669.1:p.Glu625=
XM_011529368.1:c.1915G=	XP_011527670.1:p.Glu639=
XM_011529369.1:c.1883G=	XP_011527671.1:p.Arg628=
XM_011529370.1:c.1883G=	XP_011527672.1:p.Arg628=
XM_011529373.1:c.913G=	XP_011527675.1:p.Glu305=
XR_937151.1:n.2019G=
XR_937152.1:n.2019G=
XR_937153.1:n.1900G=
XR_937154.1:n.1900G=
XR_937155.1:n.1821G=
XR_937157.1:n.1823G=
NM_001282447.2:c.1876G=	NP_001269376.1:p.Glu626=
NM_025220.4:c.1876G=	NP_079496.1:p.Glu626=
NM_153202.3:c.1876G=	NP_694882.1:p.Glu626=
XM_011529373.2:c.913G=	XP_011527675.1:p.Glu305=
XR_001754405.1:n.1987G=
XR_002958534.1:n.2096G=
NM_001282447.3:c.1876G=	NP_001269376.1:p.Glu626=
NM_025220.5:c.1876G= MANE Select	NP_079496.1:p.Glu626=
NM_153202.4:c.1876G=	NP_694882.1:p.Glu626=