Canonical Allele Identifier: CA2346678922

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671897G= , CM000682.2:g.3671897G=	GRCh38
NC_000020.10:g.3652544G= , CM000682.1:g.3652544G=	GRCh37
NC_000020.9:g.3600544G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1686C= MANE Select	ENSP00000348912.3:p.His562=
ENST00000350009.6:c.1686C=	ENSP00000322550.5:p.His562=
ENST00000356518.6:c.1686C=	ENSP00000348912.2:p.His562=
ENST00000379861.8:c.1686C=	ENSP00000369190.4:p.His562=
ENST00000466620.5:n.1325C=
ENST00000617732.1:c.*632-440C=	ENSP00000483343.1:n.*632-440C=
ENST00000619289.4:c.1326C=	ENSP00000484600.1:p.His442=
NM_001282447.1:c.1686C=	NP_001269376.1:p.His562=
NM_025220.3:c.1686C=	NP_079496.1:p.His562=
NM_153202.2:c.1686C=	NP_694882.1:p.His562=
XM_005260843.1:c.1725C=	XP_005260900.1:p.His575=
XM_006723639.1:c.1725C=	XP_006723702.1:p.His575=
XM_006723640.1:c.1716C=	XP_006723703.1:p.His572=
XM_011529366.1:c.1722C=	XP_011527668.1:p.His574=
XM_011529367.1:c.1683C=	XP_011527669.1:p.His561=
XM_011529368.1:c.1725C=	XP_011527670.1:p.His575=
XM_011529369.1:c.1693C=	XP_011527671.1:p.Leu565=
XM_011529370.1:c.1693C=	XP_011527672.1:p.Leu565=
XM_011529373.1:c.723C=	XP_011527675.1:p.His241=
XR_937151.1:n.1829C=
XR_937152.1:n.1829C=
XR_937153.1:n.1710C=
XR_937154.1:n.1710C=
XR_937155.1:n.1631C=
XR_937157.1:n.1633C=
NM_001282447.2:c.1686C=	NP_001269376.1:p.His562=
NM_025220.4:c.1686C=	NP_079496.1:p.His562=
NM_153202.3:c.1686C=	NP_694882.1:p.His562=
XM_011529373.2:c.723C=	XP_011527675.1:p.His241=
XR_001754405.1:n.1797C=
XR_002958534.1:n.1906C=
NM_001282447.3:c.1686C=	NP_001269376.1:p.His562=
NM_025220.5:c.1686C= MANE Select	NP_079496.1:p.His562=
NM_153202.4:c.1686C=	NP_694882.1:p.His562=