Canonical Allele Identifier: CA2346677692

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669577G= , CM000682.2:g.3669577G=	GRCh38
NC_000020.10:g.3650224G= , CM000682.1:g.3650224G=	GRCh37
NC_000020.9:g.3598224G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2301C= MANE Select	ENSP00000348912.3:p.Gly767=
ENST00000350009.6:c.2223C=	ENSP00000322550.5:p.Gly741=
ENST00000356518.6:c.2301C=	ENSP00000348912.2:p.Gly767=
ENST00000379861.8:c.2301C=	ENSP00000369190.4:p.Gly767=
ENST00000466620.5:n.1862C=
ENST00000483362.1:n.1049C=
ENST00000617732.1:c.*988C=	ENSP00000483343.1:n.*988C=
ENST00000619289.4:c.1941C=	ENSP00000484600.1:p.Gly647=
NM_001282447.1:c.2301C=	NP_001269376.1:p.Gly767=
NM_025220.3:c.2301C=	NP_079496.1:p.Gly767=
NM_153202.2:c.2223C=	NP_694882.1:p.Gly741=
XM_005260843.1:c.2340C=	XP_005260900.1:p.Gly780=
XM_006723639.1:c.2340C=	XP_006723702.1:p.Gly780=
XM_006723640.1:c.2331C=	XP_006723703.1:p.Gly777=
XM_011529366.1:c.2337C=	XP_011527668.1:p.Gly779=
XM_011529367.1:c.2298C=	XP_011527669.1:p.Gly766=
XM_011529368.1:c.2262C=	XP_011527670.1:p.Gly754=
XM_011529373.1:c.1338C=	XP_011527675.1:p.Gly446=
XR_937151.1:n.2384-207C=
XR_937152.1:n.2384-207C=
XR_937153.1:n.2325C=
XR_937154.1:n.2325C=
XR_937155.1:n.2246C=
XR_937157.1:n.2248C=
NM_001282447.2:c.2301C=	NP_001269376.1:p.Gly767=
NM_025220.4:c.2301C=	NP_079496.1:p.Gly767=
NM_153202.3:c.2223C=	NP_694882.1:p.Gly741=
XM_011529373.2:c.1338C=	XP_011527675.1:p.Gly446=
XR_001754405.1:n.2412C=
XR_002958534.1:n.2521C=
NM_001282447.3:c.2301C=	NP_001269376.1:p.Gly767=
NM_025220.5:c.2301C= MANE Select	NP_079496.1:p.Gly767=
NM_153202.4:c.2223C=	NP_694882.1:p.Gly741=