Canonical Allele Identifier: CA2346677576

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669334T= , CM000682.2:g.3669334T=	GRCh38
NC_000020.10:g.3649981T= , CM000682.1:g.3649981T=	GRCh37
NC_000020.9:g.3597981T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2369A= MANE Select	ENSP00000348912.3:p.Glu790=
ENST00000350009.6:c.2291A=	ENSP00000322550.5:p.Glu764=
ENST00000356518.6:c.2369A=	ENSP00000348912.2:p.Glu790=
ENST00000379861.8:c.2369A=	ENSP00000369190.4:p.Glu790=
ENST00000466620.5:n.1930A=
ENST00000483362.1:n.1292A=
ENST00000617732.1:c.*1056A=	ENSP00000483343.1:n.*1056A=
ENST00000619289.4:c.2009A=	ENSP00000484600.1:p.Glu670=
NM_001282447.1:c.2369A=	NP_001269376.1:p.Glu790=
NM_025220.3:c.2369A=	NP_079496.1:p.Glu790=
NM_153202.2:c.2291A=	NP_694882.1:p.Glu764=
XM_005260843.1:c.2408A=	XP_005260900.1:p.Glu803=
XM_006723639.1:c.2408A=	XP_006723702.1:p.Glu803=
XM_006723640.1:c.2399A=	XP_006723703.1:p.Glu800=
XM_011529366.1:c.2405A=	XP_011527668.1:p.Glu802=
XM_011529367.1:c.2366A=	XP_011527669.1:p.Glu789=
XM_011529368.1:c.2330A=	XP_011527670.1:p.Glu777=
XM_011529373.1:c.1406A=	XP_011527675.1:p.Glu469=
XR_937151.1:n.2420A=
XR_937152.1:n.2420A=
XR_937153.1:n.2393A=
XR_937154.1:n.2393A=
XR_937155.1:n.2314A=
XR_937157.1:n.2316A=
NM_001282447.2:c.2369A=	NP_001269376.1:p.Glu790=
NM_025220.4:c.2369A=	NP_079496.1:p.Glu790=
NM_153202.3:c.2291A=	NP_694882.1:p.Glu764=
XM_011529373.2:c.1406A=	XP_011527675.1:p.Glu469=
XR_001754405.1:n.2480A=
XR_002958534.1:n.2589A=
NM_001282447.3:c.2369A=	NP_001269376.1:p.Glu790=
NM_025220.5:c.2369A= MANE Select	NP_079496.1:p.Glu790=
NM_153202.4:c.2291A=	NP_694882.1:p.Glu764=