Canonical Allele Identifier: CA2346678195

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3670529G= , CM000682.2:g.3670529G=	GRCh38
NC_000020.10:g.3651176G= , CM000682.1:g.3651176G=	GRCh37
NC_000020.9:g.3599176G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2240+477C= MANE Select	ENSP00000348912.3:n.2240+477C=
ENST00000350009.6:c.2162+477C=	ENSP00000322550.5:n.2162+477C=
ENST00000356518.6:c.2240+477C=	ENSP00000348912.2:n.2240+477C=
ENST00000379861.8:c.2240+477C=	ENSP00000369190.4:n.2240+477C=
ENST00000466620.5:n.1801+477C=
ENST00000483362.1:n.97C=
ENST00000617732.1:c.*927+477C=	ENSP00000483343.1:n.*927+477C=
ENST00000619289.4:c.1880+477C=	ENSP00000484600.1:n.1880+477C=
NM_001282447.1:c.2240+477C=	NP_001269376.1:n.2240+477C=
NM_025220.3:c.2240+477C=	NP_079496.1:n.2240+477C=
NM_153202.2:c.2162+477C=	NP_694882.1:n.2162+477C=
XM_005260843.1:c.2279+477C=	XP_005260900.1:n.2279+477C=
XM_006723639.1:c.2279+477C=	XP_006723702.1:n.2279+477C=
XM_006723640.1:c.2270+477C=	XP_006723703.1:n.2270+477C=
XM_011529366.1:c.2276+477C=	XP_011527668.1:n.2276+477C=
XM_011529367.1:c.2237+477C=	XP_011527669.1:n.2237+477C=
XM_011529368.1:c.2201+477C=	XP_011527670.1:n.2201+477C=
XM_011529373.1:c.1277+477C=	XP_011527675.1:n.1277+477C=
XR_937151.1:n.2383+477C=
XR_937152.1:n.2383+477C=
XR_937153.1:n.2264+477C=
XR_937154.1:n.2264+477C=
XR_937155.1:n.2185+477C=
XR_937157.1:n.2187+477C=
NM_001282447.2:c.2240+477C=	NP_001269376.1:n.2240+477C=
NM_025220.4:c.2240+477C=	NP_079496.1:n.2240+477C=
NM_153202.3:c.2162+477C=	NP_694882.1:n.2162+477C=
XM_011529373.2:c.1277+477C=	XP_011527675.1:n.1277+477C=
XR_001754405.1:n.2351+477C=
XR_002958534.1:n.2460+477C=
NM_001282447.3:c.2240+477C=	NP_001269376.1:n.2240+477C=
NM_025220.5:c.2240+477C= MANE Select	NP_079496.1:n.2240+477C=
NM_153202.4:c.2162+477C=	NP_694882.1:n.2162+477C=