Canonical Allele Identifier: CA2346678819

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671711G= , CM000682.2:g.3671711G=	GRCh38
NC_000020.10:g.3652358G= , CM000682.1:g.3652358G=	GRCh37
NC_000020.9:g.3600358G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1775C= MANE Select	ENSP00000348912.3:p.Pro592=
ENST00000350009.6:c.1775C=	ENSP00000322550.5:p.Pro592=
ENST00000356518.6:c.1775C=	ENSP00000348912.2:p.Pro592=
ENST00000379861.8:c.1775C=	ENSP00000369190.4:p.Pro592=
ENST00000466620.5:n.1414C=
ENST00000617732.1:c.*632-254C=	ENSP00000483343.1:n.*632-254C=
ENST00000619289.4:c.1415C=	ENSP00000484600.1:p.Pro472=
NM_001282447.1:c.1775C=	NP_001269376.1:p.Pro592=
NM_025220.3:c.1775C=	NP_079496.1:p.Pro592=
NM_153202.2:c.1775C=	NP_694882.1:p.Pro592=
XM_005260843.1:c.1814C=	XP_005260900.1:p.Pro605=
XM_006723639.1:c.1814C=	XP_006723702.1:p.Pro605=
XM_006723640.1:c.1805C=	XP_006723703.1:p.Pro602=
XM_011529366.1:c.1811C=	XP_011527668.1:p.Pro604=
XM_011529367.1:c.1772C=	XP_011527669.1:p.Pro591=
XM_011529368.1:c.1814C=	XP_011527670.1:p.Pro605=
XM_011529369.1:c.1782C=	XP_011527671.1:p.Ala594=
XM_011529370.1:c.1782C=	XP_011527672.1:p.Ala594=
XM_011529373.1:c.812C=	XP_011527675.1:p.Pro271=
XR_937151.1:n.1918C=
XR_937152.1:n.1918C=
XR_937153.1:n.1799C=
XR_937154.1:n.1799C=
XR_937155.1:n.1720C=
XR_937157.1:n.1722C=
NM_001282447.2:c.1775C=	NP_001269376.1:p.Pro592=
NM_025220.4:c.1775C=	NP_079496.1:p.Pro592=
NM_153202.3:c.1775C=	NP_694882.1:p.Pro592=
XM_011529373.2:c.812C=	XP_011527675.1:p.Pro271=
XR_001754405.1:n.1886C=
XR_002958534.1:n.1995C=
NM_001282447.3:c.1775C=	NP_001269376.1:p.Pro592=
NM_025220.5:c.1775C= MANE Select	NP_079496.1:p.Pro592=
NM_153202.4:c.1775C=	NP_694882.1:p.Pro592=