Canonical Allele Identifier: CA2346677717

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669614T= , CM000682.2:g.3669614T=	GRCh38
NC_000020.10:g.3650261T= , CM000682.1:g.3650261T=	GRCh37
NC_000020.9:g.3598261T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2264A= MANE Select	ENSP00000348912.3:p.Asp755=
ENST00000350009.6:c.2186A=	ENSP00000322550.5:p.Asp729=
ENST00000356518.6:c.2264A=	ENSP00000348912.2:p.Asp755=
ENST00000379861.8:c.2264A=	ENSP00000369190.4:p.Asp755=
ENST00000466620.5:n.1825A=
ENST00000483362.1:n.1012A=
ENST00000617732.1:c.*951A=	ENSP00000483343.1:n.*951A=
ENST00000619289.4:c.1904A=	ENSP00000484600.1:p.Asp635=
NM_001282447.1:c.2264A=	NP_001269376.1:p.Asp755=
NM_025220.3:c.2264A=	NP_079496.1:p.Asp755=
NM_153202.2:c.2186A=	NP_694882.1:p.Asp729=
XM_005260843.1:c.2303A=	XP_005260900.1:p.Asp768=
XM_006723639.1:c.2303A=	XP_006723702.1:p.Asp768=
XM_006723640.1:c.2294A=	XP_006723703.1:p.Asp765=
XM_011529366.1:c.2300A=	XP_011527668.1:p.Asp767=
XM_011529367.1:c.2261A=	XP_011527669.1:p.Asp754=
XM_011529368.1:c.2225A=	XP_011527670.1:p.Asp742=
XM_011529373.1:c.1301A=	XP_011527675.1:p.Asp434=
XR_937151.1:n.2384-244A=
XR_937152.1:n.2384-244A=
XR_937153.1:n.2288A=
XR_937154.1:n.2288A=
XR_937155.1:n.2209A=
XR_937157.1:n.2211A=
NM_001282447.2:c.2264A=	NP_001269376.1:p.Asp755=
NM_025220.4:c.2264A=	NP_079496.1:p.Asp755=
NM_153202.3:c.2186A=	NP_694882.1:p.Asp729=
XM_011529373.2:c.1301A=	XP_011527675.1:p.Asp434=
XR_001754405.1:n.2375A=
XR_002958534.1:n.2484A=
NM_001282447.3:c.2264A=	NP_001269376.1:p.Asp755=
NM_025220.5:c.2264A= MANE Select	NP_079496.1:p.Asp755=
NM_153202.4:c.2186A=	NP_694882.1:p.Asp729=