Canonical Allele Identifier: CA2346678434

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671012C= , CM000682.2:g.3671012C=	GRCh38
NC_000020.10:g.3651659C= , CM000682.1:g.3651659C=	GRCh37
NC_000020.9:g.3599659C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2234G= MANE Select	ENSP00000348912.3:p.Cys745=
ENST00000350009.6:c.2156G=	ENSP00000322550.5:p.Cys719=
ENST00000356518.6:c.2234G=	ENSP00000348912.2:p.Cys745=
ENST00000379861.8:c.2234G=	ENSP00000369190.4:p.Cys745=
ENST00000466620.5:n.1795G=
ENST00000617732.1:c.*921G=	ENSP00000483343.1:n.*921G=
ENST00000619289.4:c.1874G=	ENSP00000484600.1:p.Cys625=
NM_001282447.1:c.2234G=	NP_001269376.1:p.Cys745=
NM_025220.3:c.2234G=	NP_079496.1:p.Cys745=
NM_153202.2:c.2156G=	NP_694882.1:p.Cys719=
XM_005260843.1:c.2273G=	XP_005260900.1:p.Cys758=
XM_006723639.1:c.2273G=	XP_006723702.1:p.Cys758=
XM_006723640.1:c.2264G=	XP_006723703.1:p.Cys755=
XM_011529366.1:c.2270G=	XP_011527668.1:p.Cys757=
XM_011529367.1:c.2231G=	XP_011527669.1:p.Cys744=
XM_011529368.1:c.2195G=	XP_011527670.1:p.Cys732=
XM_011529373.1:c.1271G=	XP_011527675.1:p.Cys424=
XR_937151.1:n.2377G=
XR_937152.1:n.2377G=
XR_937153.1:n.2258G=
XR_937154.1:n.2258G=
XR_937155.1:n.2179G=
XR_937157.1:n.2181G=
NM_001282447.2:c.2234G=	NP_001269376.1:p.Cys745=
NM_025220.4:c.2234G=	NP_079496.1:p.Cys745=
NM_153202.3:c.2156G=	NP_694882.1:p.Cys719=
XM_011529373.2:c.1271G=	XP_011527675.1:p.Cys424=
XR_001754405.1:n.2345G=
XR_002958534.1:n.2454G=
NM_001282447.3:c.2234G=	NP_001269376.1:p.Cys745=
NM_025220.5:c.2234G= MANE Select	NP_079496.1:p.Cys745=
NM_153202.4:c.2156G=	NP_694882.1:p.Cys719=