Canonical Allele Identifier: CA2346678852

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671778C= , CM000682.2:g.3671778C=	GRCh38
NC_000020.10:g.3652425C= , CM000682.1:g.3652425C=	GRCh37
NC_000020.9:g.3600425C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1708G= MANE Select	ENSP00000348912.3:p.Asp570=
ENST00000350009.6:c.1708G=	ENSP00000322550.5:p.Asp570=
ENST00000356518.6:c.1708G=	ENSP00000348912.2:p.Asp570=
ENST00000379861.8:c.1708G=	ENSP00000369190.4:p.Asp570=
ENST00000466620.5:n.1347G=
ENST00000617732.1:c.*632-321G=	ENSP00000483343.1:n.*632-321G=
ENST00000619289.4:c.1348G=	ENSP00000484600.1:p.Asp450=
NM_001282447.1:c.1708G=	NP_001269376.1:p.Asp570=
NM_025220.3:c.1708G=	NP_079496.1:p.Asp570=
NM_153202.2:c.1708G=	NP_694882.1:p.Asp570=
XM_005260843.1:c.1747G=	XP_005260900.1:p.Asp583=
XM_006723639.1:c.1747G=	XP_006723702.1:p.Asp583=
XM_006723640.1:c.1738G=	XP_006723703.1:p.Asp580=
XM_011529366.1:c.1744G=	XP_011527668.1:p.Asp582=
XM_011529367.1:c.1705G=	XP_011527669.1:p.Asp569=
XM_011529368.1:c.1747G=	XP_011527670.1:p.Asp583=
XM_011529369.1:c.1715G=	XP_011527671.1:p.Gly572=
XM_011529370.1:c.1715G=	XP_011527672.1:p.Gly572=
XM_011529373.1:c.745G=	XP_011527675.1:p.Asp249=
XR_937151.1:n.1851G=
XR_937152.1:n.1851G=
XR_937153.1:n.1732G=
XR_937154.1:n.1732G=
XR_937155.1:n.1653G=
XR_937157.1:n.1655G=
NM_001282447.2:c.1708G=	NP_001269376.1:p.Asp570=
NM_025220.4:c.1708G=	NP_079496.1:p.Asp570=
NM_153202.3:c.1708G=	NP_694882.1:p.Asp570=
XM_011529373.2:c.745G=	XP_011527675.1:p.Asp249=
XR_001754405.1:n.1819G=
XR_002958534.1:n.1928G=
NM_001282447.3:c.1708G=	NP_001269376.1:p.Asp570=
NM_025220.5:c.1708G= MANE Select	NP_079496.1:p.Asp570=
NM_153202.4:c.1708G=	NP_694882.1:p.Asp570=