Canonical Allele Identifier: CA2346677709

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669603C= , CM000682.2:g.3669603C=	GRCh38
NC_000020.10:g.3650250C= , CM000682.1:g.3650250C=	GRCh37
NC_000020.9:g.3598250C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2275G= MANE Select	ENSP00000348912.3:p.Gly759=
ENST00000350009.6:c.2197G=	ENSP00000322550.5:p.Gly733=
ENST00000356518.6:c.2275G=	ENSP00000348912.2:p.Gly759=
ENST00000379861.8:c.2275G=	ENSP00000369190.4:p.Gly759=
ENST00000466620.5:n.1836G=
ENST00000483362.1:n.1023G=
ENST00000617732.1:c.*962G=	ENSP00000483343.1:n.*962G=
ENST00000619289.4:c.1915G=	ENSP00000484600.1:p.Gly639=
NM_001282447.1:c.2275G=	NP_001269376.1:p.Gly759=
NM_025220.3:c.2275G=	NP_079496.1:p.Gly759=
NM_153202.2:c.2197G=	NP_694882.1:p.Gly733=
XM_005260843.1:c.2314G=	XP_005260900.1:p.Gly772=
XM_006723639.1:c.2314G=	XP_006723702.1:p.Gly772=
XM_006723640.1:c.2305G=	XP_006723703.1:p.Gly769=
XM_011529366.1:c.2311G=	XP_011527668.1:p.Gly771=
XM_011529367.1:c.2272G=	XP_011527669.1:p.Gly758=
XM_011529368.1:c.2236G=	XP_011527670.1:p.Gly746=
XM_011529373.1:c.1312G=	XP_011527675.1:p.Gly438=
XR_937151.1:n.2384-233G=
XR_937152.1:n.2384-233G=
XR_937153.1:n.2299G=
XR_937154.1:n.2299G=
XR_937155.1:n.2220G=
XR_937157.1:n.2222G=
NM_001282447.2:c.2275G=	NP_001269376.1:p.Gly759=
NM_025220.4:c.2275G=	NP_079496.1:p.Gly759=
NM_153202.3:c.2197G=	NP_694882.1:p.Gly733=
XM_011529373.2:c.1312G=	XP_011527675.1:p.Gly438=
XR_001754405.1:n.2386G=
XR_002958534.1:n.2495G=
NM_001282447.3:c.2275G=	NP_001269376.1:p.Gly759=
NM_025220.5:c.2275G= MANE Select	NP_079496.1:p.Gly759=
NM_153202.4:c.2197G=	NP_694882.1:p.Gly733=