Canonical Allele Identifier: CA2346678681

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671461G= , CM000682.2:g.3671461G=	GRCh38
NC_000020.10:g.3652108G= , CM000682.1:g.3652108G=	GRCh37
NC_000020.9:g.3600108G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.1941C= MANE Select	ENSP00000348912.3:p.Phe647=
ENST00000350009.6:c.1906-116C=	ENSP00000322550.5:n.1906-116C=
ENST00000356518.6:c.1941C=	ENSP00000348912.2:p.Phe647=
ENST00000379861.8:c.1941C=	ENSP00000369190.4:p.Phe647=
ENST00000466620.5:n.1545-116C=
ENST00000617732.1:c.*632-4C=	ENSP00000483343.1:n.*632-4C=
ENST00000619289.4:c.1581C=	ENSP00000484600.1:p.Phe527=
NM_001282447.1:c.1941C=	NP_001269376.1:p.Phe647=
NM_025220.3:c.1941C=	NP_079496.1:p.Phe647=
NM_153202.2:c.1906-116C=	NP_694882.1:n.1906-116C=
XM_005260843.1:c.1980C=	XP_005260900.1:p.Phe660=
XM_006723639.1:c.1980C=	XP_006723702.1:p.Phe660=
XM_006723640.1:c.1971C=	XP_006723703.1:p.Phe657=
XM_011529366.1:c.1977C=	XP_011527668.1:p.Phe659=
XM_011529367.1:c.1938C=	XP_011527669.1:p.Phe646=
XM_011529368.1:c.1945-116C=	XP_011527670.1:n.1945-116C=
XM_011529369.1:c.*40C=	XP_011527671.1:n.*40C=
XM_011529370.1:c.*5-116C=	XP_011527672.1:n.*5-116C=
XM_011529373.1:c.978C=	XP_011527675.1:p.Phe326=
XR_937151.1:n.2084C=
XR_937152.1:n.2084C=
XR_937153.1:n.1965C=
XR_937154.1:n.1965C=
XR_937155.1:n.1886C=
XR_937157.1:n.1888C=
NM_001282447.2:c.1941C=	NP_001269376.1:p.Phe647=
NM_025220.4:c.1941C=	NP_079496.1:p.Phe647=
NM_153202.3:c.1906-116C=	NP_694882.1:n.1906-116C=
XM_011529373.2:c.978C=	XP_011527675.1:p.Phe326=
XR_001754405.1:n.2052C=
XR_002958534.1:n.2161C=
NM_001282447.3:c.1941C=	NP_001269376.1:p.Phe647=
NM_025220.5:c.1941C= MANE Select	NP_079496.1:p.Phe647=
NM_153202.4:c.1906-116C=	NP_694882.1:n.1906-116C=