Canonical Allele Identifier: CA2346677615

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669412G= , CM000682.2:g.3669412G=	GRCh38
NC_000020.10:g.3650059G= , CM000682.1:g.3650059G=	GRCh37
NC_000020.9:g.3598059G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2333-42C= MANE Select	ENSP00000348912.3:n.2333-42C=
ENST00000350009.6:c.2255-42C=	ENSP00000322550.5:n.2255-42C=
ENST00000356518.6:c.2333-42C=	ENSP00000348912.2:n.2333-42C=
ENST00000379861.8:c.2333-42C=	ENSP00000369190.4:n.2333-42C=
ENST00000466620.5:n.1894-42C=
ENST00000483362.1:n.1214C=
ENST00000617732.1:c.*1020-42C=	ENSP00000483343.1:n.*1020-42C=
ENST00000619289.4:c.1973-42C=	ENSP00000484600.1:n.1973-42C=
NM_001282447.1:c.2333-42C=	NP_001269376.1:n.2333-42C=
NM_025220.3:c.2333-42C=	NP_079496.1:n.2333-42C=
NM_153202.2:c.2255-42C=	NP_694882.1:n.2255-42C=
XM_005260843.1:c.2372-42C=	XP_005260900.1:n.2372-42C=
XM_006723639.1:c.2372-42C=	XP_006723702.1:n.2372-42C=
XM_006723640.1:c.2363-42C=	XP_006723703.1:n.2363-42C=
XM_011529366.1:c.2369-42C=	XP_011527668.1:n.2369-42C=
XM_011529367.1:c.2330-42C=	XP_011527669.1:n.2330-42C=
XM_011529368.1:c.2294-42C=	XP_011527670.1:n.2294-42C=
XM_011529373.1:c.1370-42C=	XP_011527675.1:n.1370-42C=
XR_937151.1:n.2384-42C=
XR_937152.1:n.2384-42C=
XR_937153.1:n.2357-42C=
XR_937154.1:n.2357-42C=
XR_937155.1:n.2278-42C=
XR_937157.1:n.2280-42C=
NM_001282447.2:c.2333-42C=	NP_001269376.1:n.2333-42C=
NM_025220.4:c.2333-42C=	NP_079496.1:n.2333-42C=
NM_153202.3:c.2255-42C=	NP_694882.1:n.2255-42C=
XM_011529373.2:c.1370-42C=	XP_011527675.1:n.1370-42C=
XR_001754405.1:n.2444-42C=
XR_002958534.1:n.2553-42C=
NM_001282447.3:c.2333-42C=	NP_001269376.1:n.2333-42C=
NM_025220.5:c.2333-42C= MANE Select	NP_079496.1:n.2333-42C=
NM_153202.4:c.2255-42C=	NP_694882.1:n.2255-42C=