Canonical Allele Identifier: CA2346678818

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671709_3671712delinsCTGG , CM000682.2:g.3671709_3671712delinsCTGG	GRCh38
NC_000020.10:g.3652356_3652359delinsCTGG , CM000682.1:g.3652356_3652359delinsCTGG	GRCh37
NC_000020.9:g.3600356_3600359delinsCTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1774_1777delinsCCAG MANE Select	ENSP00000348912.3:p.Pro592=
ENST00000350009.6:c.1774_1777delinsCCAG	ENSP00000322550.5:p.Pro592=
ENST00000356518.6:c.1774_1777delinsCCAG	ENSP00000348912.2:p.Pro592=
ENST00000379861.8:c.1774_1777delinsCCAG	ENSP00000369190.4:p.Pro592=
ENST00000466620.5:n.1413_1416delinsCCAG
ENST00000617732.1:c.*632-255_*632-252delinsCCAG	ENSP00000483343.1:n.*632-255_*632-252delinsCCAG
ENST00000619289.4:c.1414_1417delinsCCAG	ENSP00000484600.1:p.Pro472=
NM_001282447.1:c.1774_1777delinsCCAG	NP_001269376.1:p.Pro592=
NM_025220.3:c.1774_1777delinsCCAG	NP_079496.1:p.Pro592=
NM_153202.2:c.1774_1777delinsCCAG	NP_694882.1:p.Pro592=
XM_005260843.1:c.1813_1816delinsCCAG	XP_005260900.1:p.Pro605=
XM_006723639.1:c.1813_1816delinsCCAG	XP_006723702.1:p.Pro605=
XM_006723640.1:c.1804_1807delinsCCAG	XP_006723703.1:p.Pro602=
XM_011529366.1:c.1810_1813delinsCCAG	XP_011527668.1:p.Pro604=
XM_011529367.1:c.1771_1774delinsCCAG	XP_011527669.1:p.Pro591=
XM_011529368.1:c.1813_1816delinsCCAG	XP_011527670.1:p.Pro605=
XM_011529369.1:c.1781_1784delinsCCAG	XP_011527671.1:p.Ala594=
XM_011529370.1:c.1781_1784delinsCCAG	XP_011527672.1:p.Ala594=
XM_011529373.1:c.811_814delinsCCAG	XP_011527675.1:p.Pro271=
XR_937151.1:n.1917_1920delinsCCAG
XR_937152.1:n.1917_1920delinsCCAG
XR_937153.1:n.1798_1801delinsCCAG
XR_937154.1:n.1798_1801delinsCCAG
XR_937155.1:n.1719_1722delinsCCAG
XR_937157.1:n.1721_1724delinsCCAG
NM_001282447.2:c.1774_1777delinsCCAG	NP_001269376.1:p.Pro592=
NM_025220.4:c.1774_1777delinsCCAG	NP_079496.1:p.Pro592=
NM_153202.3:c.1774_1777delinsCCAG	NP_694882.1:p.Pro592=
XM_011529373.2:c.811_814delinsCCAG	XP_011527675.1:p.Pro271=
XR_001754405.1:n.1885_1888delinsCCAG
XR_002958534.1:n.1994_1997delinsCCAG
NM_001282447.3:c.1774_1777delinsCCAG	NP_001269376.1:p.Pro592=
NM_025220.5:c.1774_1777delinsCCAG MANE Select	NP_079496.1:p.Pro592=
NM_153202.4:c.1774_1777delinsCCAG	NP_694882.1:p.Pro592=