Canonical Allele Identifier: CA2346678644

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671398C= , CM000682.2:g.3671398C=	GRCh38
NC_000020.10:g.3652045C= , CM000682.1:g.3652045C=	GRCh37
NC_000020.9:g.3600045C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1983+21G= MANE Select	ENSP00000348912.3:n.1983+21G=
ENST00000350009.6:c.1906-53G=	ENSP00000322550.5:n.1906-53G=
ENST00000356518.6:c.1983+21G=	ENSP00000348912.2:n.1983+21G=
ENST00000379861.8:c.1983+21G=	ENSP00000369190.4:n.1983+21G=
ENST00000466620.5:n.1545-53G=
ENST00000617732.1:c.*670+21G=	ENSP00000483343.1:n.*670+21G=
ENST00000619289.4:c.1623+21G=	ENSP00000484600.1:n.1623+21G=
NM_001282447.1:c.1983+21G=	NP_001269376.1:n.1983+21G=
NM_025220.3:c.1983+21G=	NP_079496.1:n.1983+21G=
NM_153202.2:c.1906-53G=	NP_694882.1:n.1906-53G=
XM_005260843.1:c.2022+21G=	XP_005260900.1:n.2022+21G=
XM_006723639.1:c.2022+21G=	XP_006723702.1:n.2022+21G=
XM_006723640.1:c.2013+21G=	XP_006723703.1:n.2013+21G=
XM_011529366.1:c.2019+21G=	XP_011527668.1:n.2019+21G=
XM_011529367.1:c.1980+21G=	XP_011527669.1:n.1980+21G=
XM_011529368.1:c.1945-53G=	XP_011527670.1:n.1945-53G=
XM_011529370.1:c.*5-53G=	XP_011527672.1:n.*5-53G=
XM_011529373.1:c.1020+21G=	XP_011527675.1:n.1020+21G=
XR_937151.1:n.2126+21G=
XR_937152.1:n.2126+21G=
XR_937153.1:n.2007+21G=
XR_937154.1:n.2007+21G=
XR_937155.1:n.1928+21G=
XR_937157.1:n.1930+21G=
NM_001282447.2:c.1983+21G=	NP_001269376.1:n.1983+21G=
NM_025220.4:c.1983+21G=	NP_079496.1:n.1983+21G=
NM_153202.3:c.1906-53G=	NP_694882.1:n.1906-53G=
XM_011529373.2:c.1020+21G=	XP_011527675.1:n.1020+21G=
XR_001754405.1:n.2094+21G=
XR_002958534.1:n.2203+21G=
NM_001282447.3:c.1983+21G=	NP_001269376.1:n.1983+21G=
NM_025220.5:c.1983+21G= MANE Select	NP_079496.1:n.1983+21G=
NM_153202.4:c.1906-53G=	NP_694882.1:n.1906-53G=