Canonical Allele Identifier: CA2346677720

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669619G= , CM000682.2:g.3669619G=	GRCh38
NC_000020.10:g.3650266G= , CM000682.1:g.3650266G=	GRCh37
NC_000020.9:g.3598266G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2259C= MANE Select	ENSP00000348912.3:p.His753=
ENST00000350009.6:c.2181C=	ENSP00000322550.5:p.His727=
ENST00000356518.6:c.2259C=	ENSP00000348912.2:p.His753=
ENST00000379861.8:c.2259C=	ENSP00000369190.4:p.His753=
ENST00000466620.5:n.1820C=
ENST00000483362.1:n.1007C=
ENST00000617732.1:c.*946C=	ENSP00000483343.1:n.*946C=
ENST00000619289.4:c.1899C=	ENSP00000484600.1:p.His633=
NM_001282447.1:c.2259C=	NP_001269376.1:p.His753=
NM_025220.3:c.2259C=	NP_079496.1:p.His753=
NM_153202.2:c.2181C=	NP_694882.1:p.His727=
XM_005260843.1:c.2298C=	XP_005260900.1:p.His766=
XM_006723639.1:c.2298C=	XP_006723702.1:p.His766=
XM_006723640.1:c.2289C=	XP_006723703.1:p.His763=
XM_011529366.1:c.2295C=	XP_011527668.1:p.His765=
XM_011529367.1:c.2256C=	XP_011527669.1:p.His752=
XM_011529368.1:c.2220C=	XP_011527670.1:p.His740=
XM_011529373.1:c.1296C=	XP_011527675.1:p.His432=
XR_937151.1:n.2384-249C=
XR_937152.1:n.2384-249C=
XR_937153.1:n.2283C=
XR_937154.1:n.2283C=
XR_937155.1:n.2204C=
XR_937157.1:n.2206C=
NM_001282447.2:c.2259C=	NP_001269376.1:p.His753=
NM_025220.4:c.2259C=	NP_079496.1:p.His753=
NM_153202.3:c.2181C=	NP_694882.1:p.His727=
XM_011529373.2:c.1296C=	XP_011527675.1:p.His432=
XR_001754405.1:n.2370C=
XR_002958534.1:n.2479C=
NM_001282447.3:c.2259C=	NP_001269376.1:p.His753=
NM_025220.5:c.2259C= MANE Select	NP_079496.1:p.His753=
NM_153202.4:c.2181C=	NP_694882.1:p.His727=