Canonical Allele Identifier: CA2346678493

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671118C= , CM000682.2:g.3671118C=	GRCh38
NC_000020.10:g.3651765C= , CM000682.1:g.3651765C=	GRCh37
NC_000020.9:g.3599765C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2128G= MANE Select	NP_079496.1:p.Val710=
ENST00000356518.7:c.2128G= MANE Select	ENSP00000348912.3:p.Val710=
NM_001282447.1:c.2128G=	NP_001269376.1:p.Val710=
NM_001282447.2:c.2128G=	NP_001269376.1:p.Val710=
NM_001282447.3:c.2128G=	NP_001269376.1:p.Val710=
NM_025220.3:c.2128G=	NP_079496.1:p.Val710=
NM_025220.4:c.2128G=	NP_079496.1:p.Val710=
NM_153202.2:c.2050G=	NP_694882.1:p.Val684=
NM_153202.3:c.2050G=	NP_694882.1:p.Val684=
NM_153202.4:c.2050G=	NP_694882.1:p.Val684=
ENST00000350009.6:c.2050G=	ENSP00000322550.5:p.Val684=
ENST00000356518.6:c.2128G=	ENSP00000348912.2:p.Val710=
ENST00000379861.8:c.2128G=	ENSP00000369190.4:p.Val710=
ENST00000466620.5:n.1689G=
ENST00000617732.1:c.*815G=	ENSP00000483343.1:n.*815G=
ENST00000619289.4:c.1768G=	ENSP00000484600.1:p.Val590=
XM_005260843.1:c.2167G=	XP_005260900.1:p.Val723=
XM_006723639.1:c.2167G=	XP_006723702.1:p.Val723=
XM_006723640.1:c.2158G=	XP_006723703.1:p.Val720=
XM_011529366.1:c.2164G=	XP_011527668.1:p.Val722=
XM_011529367.1:c.2125G=	XP_011527669.1:p.Val709=
XM_011529368.1:c.2089G=	XP_011527670.1:p.Val697=
XM_011529373.1:c.1165G=	XP_011527675.1:p.Val389=
XM_011529373.2:c.1165G=	XP_011527675.1:p.Val389=
XR_001754405.1:n.2239G=
XR_002958534.1:n.2348G=
XR_937151.1:n.2271G=
XR_937152.1:n.2271G=
XR_937153.1:n.2152G=
XR_937154.1:n.2152G=
XR_937155.1:n.2073G=
XR_937157.1:n.2075G=