Canonical Allele Identifier: CA2346677680

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669557G= , CM000682.2:g.3669557G=	GRCh38
NC_000020.10:g.3650204G= , CM000682.1:g.3650204G=	GRCh37
NC_000020.9:g.3598204G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2321C= MANE Select	ENSP00000348912.3:p.Pro774=
ENST00000350009.6:c.2243C=	ENSP00000322550.5:p.Pro748=
ENST00000356518.6:c.2321C=	ENSP00000348912.2:p.Pro774=
ENST00000379861.8:c.2321C=	ENSP00000369190.4:p.Pro774=
ENST00000466620.5:n.1882C=
ENST00000483362.1:n.1069C=
ENST00000617732.1:c.*1008C=	ENSP00000483343.1:n.*1008C=
ENST00000619289.4:c.1961C=	ENSP00000484600.1:p.Pro654=
NM_001282447.1:c.2321C=	NP_001269376.1:p.Pro774=
NM_025220.3:c.2321C=	NP_079496.1:p.Pro774=
NM_153202.2:c.2243C=	NP_694882.1:p.Pro748=
XM_005260843.1:c.2360C=	XP_005260900.1:p.Pro787=
XM_006723639.1:c.2360C=	XP_006723702.1:p.Pro787=
XM_006723640.1:c.2351C=	XP_006723703.1:p.Pro784=
XM_011529366.1:c.2357C=	XP_011527668.1:p.Pro786=
XM_011529367.1:c.2318C=	XP_011527669.1:p.Pro773=
XM_011529368.1:c.2282C=	XP_011527670.1:p.Pro761=
XM_011529373.1:c.1358C=	XP_011527675.1:p.Pro453=
XR_937151.1:n.2384-187C=
XR_937152.1:n.2384-187C=
XR_937153.1:n.2345C=
XR_937154.1:n.2345C=
XR_937155.1:n.2266C=
XR_937157.1:n.2268C=
NM_001282447.2:c.2321C=	NP_001269376.1:p.Pro774=
NM_025220.4:c.2321C=	NP_079496.1:p.Pro774=
NM_153202.3:c.2243C=	NP_694882.1:p.Pro748=
XM_011529373.2:c.1358C=	XP_011527675.1:p.Pro453=
XR_001754405.1:n.2432C=
XR_002958534.1:n.2541C=
NM_001282447.3:c.2321C=	NP_001269376.1:p.Pro774=
NM_025220.5:c.2321C= MANE Select	NP_079496.1:p.Pro774=
NM_153202.4:c.2243C=	NP_694882.1:p.Pro748=