Canonical Allele Identifier: CA2346677704

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669597C= , CM000682.2:g.3669597C=	GRCh38
NC_000020.10:g.3650244C= , CM000682.1:g.3650244C=	GRCh37
NC_000020.9:g.3598244C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2281G= MANE Select	NP_079496.1:p.Val761=
ENST00000356518.7:c.2281G= MANE Select	ENSP00000348912.3:p.Val761=
NM_001282447.1:c.2281G=	NP_001269376.1:p.Val761=
NM_001282447.2:c.2281G=	NP_001269376.1:p.Val761=
NM_001282447.3:c.2281G=	NP_001269376.1:p.Val761=
NM_025220.3:c.2281G=	NP_079496.1:p.Val761=
NM_025220.4:c.2281G=	NP_079496.1:p.Val761=
NM_153202.2:c.2203G=	NP_694882.1:p.Val735=
NM_153202.3:c.2203G=	NP_694882.1:p.Val735=
NM_153202.4:c.2203G=	NP_694882.1:p.Val735=
ENST00000350009.6:c.2203G=	ENSP00000322550.5:p.Val735=
ENST00000356518.6:c.2281G=	ENSP00000348912.2:p.Val761=
ENST00000379861.8:c.2281G=	ENSP00000369190.4:p.Val761=
ENST00000466620.5:n.1842G=
ENST00000483362.1:n.1029G=
ENST00000617732.1:c.*968G=	ENSP00000483343.1:n.*968G=
ENST00000619289.4:c.1921G=	ENSP00000484600.1:p.Val641=
XM_005260843.1:c.2320G=	XP_005260900.1:p.Val774=
XM_006723639.1:c.2320G=	XP_006723702.1:p.Val774=
XM_006723640.1:c.2311G=	XP_006723703.1:p.Val771=
XM_011529366.1:c.2317G=	XP_011527668.1:p.Val773=
XM_011529367.1:c.2278G=	XP_011527669.1:p.Val760=
XM_011529368.1:c.2242G=	XP_011527670.1:p.Val748=
XM_011529373.1:c.1318G=	XP_011527675.1:p.Val440=
XM_011529373.2:c.1318G=	XP_011527675.1:p.Val440=
XR_001754405.1:n.2392G=
XR_002958534.1:n.2501G=
XR_937151.1:n.2384-227G=
XR_937152.1:n.2384-227G=
XR_937153.1:n.2305G=
XR_937154.1:n.2305G=
XR_937155.1:n.2226G=
XR_937157.1:n.2228G=