Canonical Allele Identifier: CA2346678794

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671665_3671668delinsCCGA , CM000682.2:g.3671665_3671668delinsCCGA	GRCh38
NC_000020.10:g.3652312_3652315delinsCCGA , CM000682.1:g.3652312_3652315delinsCCGA	GRCh37
NC_000020.9:g.3600312_3600315delinsCCGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1818_1821delinsTCGG MANE Select	ENSP00000348912.3:p.Cys606=
ENST00000350009.6:c.1818_1821delinsTCGG	ENSP00000322550.5:p.Cys606=
ENST00000356518.6:c.1818_1821delinsTCGG	ENSP00000348912.2:p.Cys606=
ENST00000379861.8:c.1818_1821delinsTCGG	ENSP00000369190.4:p.Cys606=
ENST00000466620.5:n.1457_1460delinsTCGG
ENST00000617732.1:c.*632-211_*632-208delinsTCGG	ENSP00000483343.1:n.*632-211_*632-208delinsTCGG
ENST00000619289.4:c.1458_1461delinsTCGG	ENSP00000484600.1:p.Cys486=
NM_001282447.1:c.1818_1821delinsTCGG	NP_001269376.1:p.Cys606=
NM_025220.3:c.1818_1821delinsTCGG	NP_079496.1:p.Cys606=
NM_153202.2:c.1818_1821delinsTCGG	NP_694882.1:p.Cys606=
XM_005260843.1:c.1857_1860delinsTCGG	XP_005260900.1:p.Cys619=
XM_006723639.1:c.1857_1860delinsTCGG	XP_006723702.1:p.Cys619=
XM_006723640.1:c.1848_1851delinsTCGG	XP_006723703.1:p.Cys616=
XM_011529366.1:c.1854_1857delinsTCGG	XP_011527668.1:p.Cys618=
XM_011529367.1:c.1815_1818delinsTCGG	XP_011527669.1:p.Cys605=
XM_011529368.1:c.1857_1860delinsTCGG	XP_011527670.1:p.Cys619=
XM_011529369.1:c.1825_1828delinsTCGG	XP_011527671.1:p.Ser609=
XM_011529370.1:c.1825_1828delinsTCGG	XP_011527672.1:p.Ser609=
XM_011529373.1:c.855_858delinsTCGG	XP_011527675.1:p.Cys285=
XR_937151.1:n.1961_1964delinsTCGG
XR_937152.1:n.1961_1964delinsTCGG
XR_937153.1:n.1842_1845delinsTCGG
XR_937154.1:n.1842_1845delinsTCGG
XR_937155.1:n.1763_1766delinsTCGG
XR_937157.1:n.1765_1768delinsTCGG
NM_001282447.2:c.1818_1821delinsTCGG	NP_001269376.1:p.Cys606=
NM_025220.4:c.1818_1821delinsTCGG	NP_079496.1:p.Cys606=
NM_153202.3:c.1818_1821delinsTCGG	NP_694882.1:p.Cys606=
XM_011529373.2:c.855_858delinsTCGG	XP_011527675.1:p.Cys285=
XR_001754405.1:n.1929_1932delinsTCGG
XR_002958534.1:n.2038_2041delinsTCGG
NM_001282447.3:c.1818_1821delinsTCGG	NP_001269376.1:p.Cys606=
NM_025220.5:c.1818_1821delinsTCGG MANE Select	NP_079496.1:p.Cys606=
NM_153202.4:c.1818_1821delinsTCGG	NP_694882.1:p.Cys606=