Canonical Allele Identifier: CA2346678825

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671720T= , CM000682.2:g.3671720T=	GRCh38
NC_000020.10:g.3652367T= , CM000682.1:g.3652367T=	GRCh37
NC_000020.9:g.3600367T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1766A= MANE Select	ENSP00000348912.3:p.His589=
ENST00000350009.6:c.1766A=	ENSP00000322550.5:p.His589=
ENST00000356518.6:c.1766A=	ENSP00000348912.2:p.His589=
ENST00000379861.8:c.1766A=	ENSP00000369190.4:p.His589=
ENST00000466620.5:n.1405A=
ENST00000617732.1:c.*632-263A=	ENSP00000483343.1:n.*632-263A=
ENST00000619289.4:c.1406A=	ENSP00000484600.1:p.His469=
NM_001282447.1:c.1766A=	NP_001269376.1:p.His589=
NM_025220.3:c.1766A=	NP_079496.1:p.His589=
NM_153202.2:c.1766A=	NP_694882.1:p.His589=
XM_005260843.1:c.1805A=	XP_005260900.1:p.His602=
XM_006723639.1:c.1805A=	XP_006723702.1:p.His602=
XM_006723640.1:c.1796A=	XP_006723703.1:p.His599=
XM_011529366.1:c.1802A=	XP_011527668.1:p.His601=
XM_011529367.1:c.1763A=	XP_011527669.1:p.His588=
XM_011529368.1:c.1805A=	XP_011527670.1:p.His602=
XM_011529369.1:c.1773A=	XP_011527671.1:p.Ala591=
XM_011529370.1:c.1773A=	XP_011527672.1:p.Ala591=
XM_011529373.1:c.803A=	XP_011527675.1:p.His268=
XR_937151.1:n.1909A=
XR_937152.1:n.1909A=
XR_937153.1:n.1790A=
XR_937154.1:n.1790A=
XR_937155.1:n.1711A=
XR_937157.1:n.1713A=
NM_001282447.2:c.1766A=	NP_001269376.1:p.His589=
NM_025220.4:c.1766A=	NP_079496.1:p.His589=
NM_153202.3:c.1766A=	NP_694882.1:p.His589=
XM_011529373.2:c.803A=	XP_011527675.1:p.His268=
XR_001754405.1:n.1877A=
XR_002958534.1:n.1986A=
NM_001282447.3:c.1766A=	NP_001269376.1:p.His589=
NM_025220.5:c.1766A= MANE Select	NP_079496.1:p.His589=
NM_153202.4:c.1766A=	NP_694882.1:p.His589=