Canonical Allele Identifier: CA2346678846

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671765C= , CM000682.2:g.3671765C=	GRCh38
NC_000020.10:g.3652412C= , CM000682.1:g.3652412C=	GRCh37
NC_000020.9:g.3600412C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1721G= MANE Select	ENSP00000348912.3:p.Gly574=
ENST00000350009.6:c.1721G=	ENSP00000322550.5:p.Gly574=
ENST00000356518.6:c.1721G=	ENSP00000348912.2:p.Gly574=
ENST00000379861.8:c.1721G=	ENSP00000369190.4:p.Gly574=
ENST00000466620.5:n.1360G=
ENST00000617732.1:c.*632-308G=	ENSP00000483343.1:n.*632-308G=
ENST00000619289.4:c.1361G=	ENSP00000484600.1:p.Gly454=
NM_001282447.1:c.1721G=	NP_001269376.1:p.Gly574=
NM_025220.3:c.1721G=	NP_079496.1:p.Gly574=
NM_153202.2:c.1721G=	NP_694882.1:p.Gly574=
XM_005260843.1:c.1760G=	XP_005260900.1:p.Gly587=
XM_006723639.1:c.1760G=	XP_006723702.1:p.Gly587=
XM_006723640.1:c.1751G=	XP_006723703.1:p.Gly584=
XM_011529366.1:c.1757G=	XP_011527668.1:p.Gly586=
XM_011529367.1:c.1718G=	XP_011527669.1:p.Gly573=
XM_011529368.1:c.1760G=	XP_011527670.1:p.Gly587=
XM_011529369.1:c.1728G=	XP_011527671.1:p.Trp576=
XM_011529370.1:c.1728G=	XP_011527672.1:p.Trp576=
XM_011529373.1:c.758G=	XP_011527675.1:p.Gly253=
XR_937151.1:n.1864G=
XR_937152.1:n.1864G=
XR_937153.1:n.1745G=
XR_937154.1:n.1745G=
XR_937155.1:n.1666G=
XR_937157.1:n.1668G=
NM_001282447.2:c.1721G=	NP_001269376.1:p.Gly574=
NM_025220.4:c.1721G=	NP_079496.1:p.Gly574=
NM_153202.3:c.1721G=	NP_694882.1:p.Gly574=
XM_011529373.2:c.758G=	XP_011527675.1:p.Gly253=
XR_001754405.1:n.1832G=
XR_002958534.1:n.1941G=
NM_001282447.3:c.1721G=	NP_001269376.1:p.Gly574=
NM_025220.5:c.1721G= MANE Select	NP_079496.1:p.Gly574=
NM_153202.4:c.1721G=	NP_694882.1:p.Gly574=