Canonical Allele Identifier: CA2346677708

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669602C= , CM000682.2:g.3669602C=	GRCh38
NC_000020.10:g.3650249C= , CM000682.1:g.3650249C=	GRCh37
NC_000020.9:g.3598249C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2276G= MANE Select	ENSP00000348912.3:p.Gly759=
ENST00000350009.6:c.2198G=	ENSP00000322550.5:p.Gly733=
ENST00000356518.6:c.2276G=	ENSP00000348912.2:p.Gly759=
ENST00000379861.8:c.2276G=	ENSP00000369190.4:p.Gly759=
ENST00000466620.5:n.1837G=
ENST00000483362.1:n.1024G=
ENST00000617732.1:c.*963G=	ENSP00000483343.1:n.*963G=
ENST00000619289.4:c.1916G=	ENSP00000484600.1:p.Gly639=
NM_001282447.1:c.2276G=	NP_001269376.1:p.Gly759=
NM_025220.3:c.2276G=	NP_079496.1:p.Gly759=
NM_153202.2:c.2198G=	NP_694882.1:p.Gly733=
XM_005260843.1:c.2315G=	XP_005260900.1:p.Gly772=
XM_006723639.1:c.2315G=	XP_006723702.1:p.Gly772=
XM_006723640.1:c.2306G=	XP_006723703.1:p.Gly769=
XM_011529366.1:c.2312G=	XP_011527668.1:p.Gly771=
XM_011529367.1:c.2273G=	XP_011527669.1:p.Gly758=
XM_011529368.1:c.2237G=	XP_011527670.1:p.Gly746=
XM_011529373.1:c.1313G=	XP_011527675.1:p.Gly438=
XR_937151.1:n.2384-232G=
XR_937152.1:n.2384-232G=
XR_937153.1:n.2300G=
XR_937154.1:n.2300G=
XR_937155.1:n.2221G=
XR_937157.1:n.2223G=
NM_001282447.2:c.2276G=	NP_001269376.1:p.Gly759=
NM_025220.4:c.2276G=	NP_079496.1:p.Gly759=
NM_153202.3:c.2198G=	NP_694882.1:p.Gly733=
XM_011529373.2:c.1313G=	XP_011527675.1:p.Gly438=
XR_001754405.1:n.2387G=
XR_002958534.1:n.2496G=
NM_001282447.3:c.2276G=	NP_001269376.1:p.Gly759=
NM_025220.5:c.2276G= MANE Select	NP_079496.1:p.Gly759=
NM_153202.4:c.2198G=	NP_694882.1:p.Gly733=