Canonical Allele Identifier: CA2346677722

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669624G= , CM000682.2:g.3669624G=	GRCh38
NC_000020.10:g.3650271G= , CM000682.1:g.3650271G=	GRCh37
NC_000020.9:g.3598271G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2254C= MANE Select	ENSP00000348912.3:p.Pro752=
ENST00000350009.6:c.2176C=	ENSP00000322550.5:p.Pro726=
ENST00000356518.6:c.2254C=	ENSP00000348912.2:p.Pro752=
ENST00000379861.8:c.2254C=	ENSP00000369190.4:p.Pro752=
ENST00000466620.5:n.1815C=
ENST00000483362.1:n.1002C=
ENST00000617732.1:c.*941C=	ENSP00000483343.1:n.*941C=
ENST00000619289.4:c.1894C=	ENSP00000484600.1:p.Pro632=
NM_001282447.1:c.2254C=	NP_001269376.1:p.Pro752=
NM_025220.3:c.2254C=	NP_079496.1:p.Pro752=
NM_153202.2:c.2176C=	NP_694882.1:p.Pro726=
XM_005260843.1:c.2293C=	XP_005260900.1:p.Pro765=
XM_006723639.1:c.2293C=	XP_006723702.1:p.Pro765=
XM_006723640.1:c.2284C=	XP_006723703.1:p.Pro762=
XM_011529366.1:c.2290C=	XP_011527668.1:p.Pro764=
XM_011529367.1:c.2251C=	XP_011527669.1:p.Pro751=
XM_011529368.1:c.2215C=	XP_011527670.1:p.Pro739=
XM_011529373.1:c.1291C=	XP_011527675.1:p.Pro431=
XR_937151.1:n.2384-254C=
XR_937152.1:n.2384-254C=
XR_937153.1:n.2278C=
XR_937154.1:n.2278C=
XR_937155.1:n.2199C=
XR_937157.1:n.2201C=
NM_001282447.2:c.2254C=	NP_001269376.1:p.Pro752=
NM_025220.4:c.2254C=	NP_079496.1:p.Pro752=
NM_153202.3:c.2176C=	NP_694882.1:p.Pro726=
XM_011529373.2:c.1291C=	XP_011527675.1:p.Pro431=
XR_001754405.1:n.2365C=
XR_002958534.1:n.2474C=
NM_001282447.3:c.2254C=	NP_001269376.1:p.Pro752=
NM_025220.5:c.2254C= MANE Select	NP_079496.1:p.Pro752=
NM_153202.4:c.2176C=	NP_694882.1:p.Pro726=