Canonical Allele Identifier: CA2346678844

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671758C= , CM000682.2:g.3671758C=	GRCh38
NC_000020.10:g.3652405C= , CM000682.1:g.3652405C=	GRCh37
NC_000020.9:g.3600405C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1728G= MANE Select	ENSP00000348912.3:p.Leu576=
ENST00000350009.6:c.1728G=	ENSP00000322550.5:p.Leu576=
ENST00000356518.6:c.1728G=	ENSP00000348912.2:p.Leu576=
ENST00000379861.8:c.1728G=	ENSP00000369190.4:p.Leu576=
ENST00000466620.5:n.1367G=
ENST00000617732.1:c.*632-301G=	ENSP00000483343.1:n.*632-301G=
ENST00000619289.4:c.1368G=	ENSP00000484600.1:p.Leu456=
NM_001282447.1:c.1728G=	NP_001269376.1:p.Leu576=
NM_025220.3:c.1728G=	NP_079496.1:p.Leu576=
NM_153202.2:c.1728G=	NP_694882.1:p.Leu576=
XM_005260843.1:c.1767G=	XP_005260900.1:p.Leu589=
XM_006723639.1:c.1767G=	XP_006723702.1:p.Leu589=
XM_006723640.1:c.1758G=	XP_006723703.1:p.Leu586=
XM_011529366.1:c.1764G=	XP_011527668.1:p.Leu588=
XM_011529367.1:c.1725G=	XP_011527669.1:p.Leu575=
XM_011529368.1:c.1767G=	XP_011527670.1:p.Leu589=
XM_011529369.1:c.1735G=	XP_011527671.1:p.Ala579=
XM_011529370.1:c.1735G=	XP_011527672.1:p.Ala579=
XM_011529373.1:c.765G=	XP_011527675.1:p.Leu255=
XR_937151.1:n.1871G=
XR_937152.1:n.1871G=
XR_937153.1:n.1752G=
XR_937154.1:n.1752G=
XR_937155.1:n.1673G=
XR_937157.1:n.1675G=
NM_001282447.2:c.1728G=	NP_001269376.1:p.Leu576=
NM_025220.4:c.1728G=	NP_079496.1:p.Leu576=
NM_153202.3:c.1728G=	NP_694882.1:p.Leu576=
XM_011529373.2:c.765G=	XP_011527675.1:p.Leu255=
XR_001754405.1:n.1839G=
XR_002958534.1:n.1948G=
NM_001282447.3:c.1728G=	NP_001269376.1:p.Leu576=
NM_025220.5:c.1728G= MANE Select	NP_079496.1:p.Leu576=
NM_153202.4:c.1728G=	NP_694882.1:p.Leu576=