Canonical Allele Identifier: CA2346677696

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669583C= , CM000682.2:g.3669583C=	GRCh38
NC_000020.10:g.3650230C= , CM000682.1:g.3650230C=	GRCh37
NC_000020.9:g.3598230C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2295G= MANE Select	ENSP00000348912.3:p.Glu765=
ENST00000350009.6:c.2217G=	ENSP00000322550.5:p.Glu739=
ENST00000356518.6:c.2295G=	ENSP00000348912.2:p.Glu765=
ENST00000379861.8:c.2295G=	ENSP00000369190.4:p.Glu765=
ENST00000466620.5:n.1856G=
ENST00000483362.1:n.1043G=
ENST00000617732.1:c.*982G=	ENSP00000483343.1:n.*982G=
ENST00000619289.4:c.1935G=	ENSP00000484600.1:p.Glu645=
NM_001282447.1:c.2295G=	NP_001269376.1:p.Glu765=
NM_025220.3:c.2295G=	NP_079496.1:p.Glu765=
NM_153202.2:c.2217G=	NP_694882.1:p.Glu739=
XM_005260843.1:c.2334G=	XP_005260900.1:p.Glu778=
XM_006723639.1:c.2334G=	XP_006723702.1:p.Glu778=
XM_006723640.1:c.2325G=	XP_006723703.1:p.Glu775=
XM_011529366.1:c.2331G=	XP_011527668.1:p.Glu777=
XM_011529367.1:c.2292G=	XP_011527669.1:p.Glu764=
XM_011529368.1:c.2256G=	XP_011527670.1:p.Glu752=
XM_011529373.1:c.1332G=	XP_011527675.1:p.Glu444=
XR_937151.1:n.2384-213G=
XR_937152.1:n.2384-213G=
XR_937153.1:n.2319G=
XR_937154.1:n.2319G=
XR_937155.1:n.2240G=
XR_937157.1:n.2242G=
NM_001282447.2:c.2295G=	NP_001269376.1:p.Glu765=
NM_025220.4:c.2295G=	NP_079496.1:p.Glu765=
NM_153202.3:c.2217G=	NP_694882.1:p.Glu739=
XM_011529373.2:c.1332G=	XP_011527675.1:p.Glu444=
XR_001754405.1:n.2406G=
XR_002958534.1:n.2515G=
NM_001282447.3:c.2295G=	NP_001269376.1:p.Glu765=
NM_025220.5:c.2295G= MANE Select	NP_079496.1:p.Glu765=
NM_153202.4:c.2217G=	NP_694882.1:p.Glu739=