Canonical Allele Identifier: CA2346677691

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669573T= , CM000682.2:g.3669573T=	GRCh38
NC_000020.10:g.3650220T= , CM000682.1:g.3650220T=	GRCh37
NC_000020.9:g.3598220T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2305A= MANE Select	ENSP00000348912.3:p.Thr769=
ENST00000350009.6:c.2227A=	ENSP00000322550.5:p.Thr743=
ENST00000356518.6:c.2305A=	ENSP00000348912.2:p.Thr769=
ENST00000379861.8:c.2305A=	ENSP00000369190.4:p.Thr769=
ENST00000466620.5:n.1866A=
ENST00000483362.1:n.1053A=
ENST00000617732.1:c.*992A=	ENSP00000483343.1:n.*992A=
ENST00000619289.4:c.1945A=	ENSP00000484600.1:p.Thr649=
NM_001282447.1:c.2305A=	NP_001269376.1:p.Thr769=
NM_025220.3:c.2305A=	NP_079496.1:p.Thr769=
NM_153202.2:c.2227A=	NP_694882.1:p.Thr743=
XM_005260843.1:c.2344A=	XP_005260900.1:p.Thr782=
XM_006723639.1:c.2344A=	XP_006723702.1:p.Thr782=
XM_006723640.1:c.2335A=	XP_006723703.1:p.Thr779=
XM_011529366.1:c.2341A=	XP_011527668.1:p.Thr781=
XM_011529367.1:c.2302A=	XP_011527669.1:p.Thr768=
XM_011529368.1:c.2266A=	XP_011527670.1:p.Thr756=
XM_011529373.1:c.1342A=	XP_011527675.1:p.Thr448=
XR_937151.1:n.2384-203A=
XR_937152.1:n.2384-203A=
XR_937153.1:n.2329A=
XR_937154.1:n.2329A=
XR_937155.1:n.2250A=
XR_937157.1:n.2252A=
NM_001282447.2:c.2305A=	NP_001269376.1:p.Thr769=
NM_025220.4:c.2305A=	NP_079496.1:p.Thr769=
NM_153202.3:c.2227A=	NP_694882.1:p.Thr743=
XM_011529373.2:c.1342A=	XP_011527675.1:p.Thr448=
XR_001754405.1:n.2416A=
XR_002958534.1:n.2525A=
NM_001282447.3:c.2305A=	NP_001269376.1:p.Thr769=
NM_025220.5:c.2305A= MANE Select	NP_079496.1:p.Thr769=
NM_153202.4:c.2227A=	NP_694882.1:p.Thr743=