Canonical Allele Identifier: CA2346677724

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669627C= , CM000682.2:g.3669627C=	GRCh38
NC_000020.10:g.3650274C= , CM000682.1:g.3650274C=	GRCh37
NC_000020.9:g.3598274C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2251G= MANE Select	ENSP00000348912.3:p.Gly751=
ENST00000350009.6:c.2173G=	ENSP00000322550.5:p.Gly725=
ENST00000356518.6:c.2251G=	ENSP00000348912.2:p.Gly751=
ENST00000379861.8:c.2251G=	ENSP00000369190.4:p.Gly751=
ENST00000466620.5:n.1812G=
ENST00000483362.1:n.999G=
ENST00000617732.1:c.*938G=	ENSP00000483343.1:n.*938G=
ENST00000619289.4:c.1891G=	ENSP00000484600.1:p.Gly631=
NM_001282447.1:c.2251G=	NP_001269376.1:p.Gly751=
NM_025220.3:c.2251G=	NP_079496.1:p.Gly751=
NM_153202.2:c.2173G=	NP_694882.1:p.Gly725=
XM_005260843.1:c.2290G=	XP_005260900.1:p.Gly764=
XM_006723639.1:c.2290G=	XP_006723702.1:p.Gly764=
XM_006723640.1:c.2281G=	XP_006723703.1:p.Gly761=
XM_011529366.1:c.2287G=	XP_011527668.1:p.Gly763=
XM_011529367.1:c.2248G=	XP_011527669.1:p.Gly750=
XM_011529368.1:c.2212G=	XP_011527670.1:p.Gly738=
XM_011529373.1:c.1288G=	XP_011527675.1:p.Gly430=
XR_937151.1:n.2384-257G=
XR_937152.1:n.2384-257G=
XR_937153.1:n.2275G=
XR_937154.1:n.2275G=
XR_937155.1:n.2196G=
XR_937157.1:n.2198G=
NM_001282447.2:c.2251G=	NP_001269376.1:p.Gly751=
NM_025220.4:c.2251G=	NP_079496.1:p.Gly751=
NM_153202.3:c.2173G=	NP_694882.1:p.Gly725=
XM_011529373.2:c.1288G=	XP_011527675.1:p.Gly430=
XR_001754405.1:n.2362G=
XR_002958534.1:n.2471G=
NM_001282447.3:c.2251G=	NP_001269376.1:p.Gly751=
NM_025220.5:c.2251G= MANE Select	NP_079496.1:p.Gly751=
NM_153202.4:c.2173G=	NP_694882.1:p.Gly725=