Canonical Allele Identifier: CA2346677649

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669502C= , CM000682.2:g.3669502C=	GRCh38
NC_000020.10:g.3650149C= , CM000682.1:g.3650149C=	GRCh37
NC_000020.9:g.3598149C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2332+44G= MANE Select	NP_079496.1:n.2332+44G=
ENST00000356518.7:c.2332+44G= MANE Select	ENSP00000348912.3:n.2332+44G=
NM_001282447.1:c.2332+44G=	NP_001269376.1:n.2332+44G=
NM_001282447.2:c.2332+44G=	NP_001269376.1:n.2332+44G=
NM_001282447.3:c.2332+44G=	NP_001269376.1:n.2332+44G=
NM_025220.3:c.2332+44G=	NP_079496.1:n.2332+44G=
NM_025220.4:c.2332+44G=	NP_079496.1:n.2332+44G=
NM_153202.2:c.2254+44G=	NP_694882.1:n.2254+44G=
NM_153202.3:c.2254+44G=	NP_694882.1:n.2254+44G=
NM_153202.4:c.2254+44G=	NP_694882.1:n.2254+44G=
ENST00000350009.6:c.2254+44G=	ENSP00000322550.5:n.2254+44G=
ENST00000356518.6:c.2332+44G=	ENSP00000348912.2:n.2332+44G=
ENST00000379861.8:c.2332+44G=	ENSP00000369190.4:n.2332+44G=
ENST00000466620.5:n.1893+44G=
ENST00000483362.1:n.1124G=
ENST00000617732.1:c.*1019+44G=	ENSP00000483343.1:n.*1019+44G=
ENST00000619289.4:c.1972+44G=	ENSP00000484600.1:n.1972+44G=
XM_005260843.1:c.2371+44G=	XP_005260900.1:n.2371+44G=
XM_006723639.1:c.2371+44G=	XP_006723702.1:n.2371+44G=
XM_006723640.1:c.2362+44G=	XP_006723703.1:n.2362+44G=
XM_011529366.1:c.2368+44G=	XP_011527668.1:n.2368+44G=
XM_011529367.1:c.2329+44G=	XP_011527669.1:n.2329+44G=
XM_011529368.1:c.2293+44G=	XP_011527670.1:n.2293+44G=
XM_011529373.1:c.1369+44G=	XP_011527675.1:n.1369+44G=
XM_011529373.2:c.1369+44G=	XP_011527675.1:n.1369+44G=
XR_001754405.1:n.2443+44G=
XR_002958534.1:n.2552+44G=
XR_937151.1:n.2384-132G=
XR_937152.1:n.2384-132G=
XR_937153.1:n.2356+44G=
XR_937154.1:n.2356+44G=
XR_937155.1:n.2277+44G=
XR_937157.1:n.2279+44G=