Canonical Allele Identifier: CA2346678757

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671602_3671603delinsGC , CM000682.2:g.3671602_3671603delinsGC	GRCh38
NC_000020.10:g.3652249_3652250delinsGC , CM000682.1:g.3652249_3652250delinsGC	GRCh37
NC_000020.9:g.3600249_3600250delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1883_1884delinsGC MANE Select	ENSP00000348912.3:p.Gly628=
ENST00000350009.6:c.1883_1884delinsGC	ENSP00000322550.5:p.Gly628=
ENST00000356518.6:c.1883_1884delinsGC	ENSP00000348912.2:p.Gly628=
ENST00000379861.8:c.1883_1884delinsGC	ENSP00000369190.4:p.Gly628=
ENST00000466620.5:n.1522_1523delinsGC
ENST00000617732.1:c.*632-146_*632-145delinsGC	ENSP00000483343.1:n.*632-146_*632-145delinsGC
ENST00000619289.4:c.1523_1524delinsGC	ENSP00000484600.1:p.Gly508=
NM_001282447.1:c.1883_1884delinsGC	NP_001269376.1:p.Gly628=
NM_025220.3:c.1883_1884delinsGC	NP_079496.1:p.Gly628=
NM_153202.2:c.1883_1884delinsGC	NP_694882.1:p.Gly628=
XM_005260843.1:c.1922_1923delinsGC	XP_005260900.1:p.Gly641=
XM_006723639.1:c.1922_1923delinsGC	XP_006723702.1:p.Gly641=
XM_006723640.1:c.1913_1914delinsGC	XP_006723703.1:p.Gly638=
XM_011529366.1:c.1919_1920delinsGC	XP_011527668.1:p.Gly640=
XM_011529367.1:c.1880_1881delinsGC	XP_011527669.1:p.Gly627=
XM_011529368.1:c.1922_1923delinsGC	XP_011527670.1:p.Gly641=
XM_011529369.1:c.1890_1891delinsGC	XP_011527671.1:p.Arg630=
XM_011529370.1:c.1890_1891delinsGC	XP_011527672.1:p.Arg630=
XM_011529373.1:c.920_921delinsGC	XP_011527675.1:p.Gly307=
XR_937151.1:n.2026_2027delinsGC
XR_937152.1:n.2026_2027delinsGC
XR_937153.1:n.1907_1908delinsGC
XR_937154.1:n.1907_1908delinsGC
XR_937155.1:n.1828_1829delinsGC
XR_937157.1:n.1830_1831delinsGC
NM_001282447.2:c.1883_1884delinsGC	NP_001269376.1:p.Gly628=
NM_025220.4:c.1883_1884delinsGC	NP_079496.1:p.Gly628=
NM_153202.3:c.1883_1884delinsGC	NP_694882.1:p.Gly628=
XM_011529373.2:c.920_921delinsGC	XP_011527675.1:p.Gly307=
XR_001754405.1:n.1994_1995delinsGC
XR_002958534.1:n.2103_2104delinsGC
NM_001282447.3:c.1883_1884delinsGC	NP_001269376.1:p.Gly628=
NM_025220.5:c.1883_1884delinsGC MANE Select	NP_079496.1:p.Gly628=
NM_153202.4:c.1883_1884delinsGC	NP_694882.1:p.Gly628=