Canonical Allele Identifier: CA2346678945

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671935_3671936delinsCT , CM000682.2:g.3671935_3671936delinsCT	GRCh38
NC_000020.10:g.3652582_3652583delinsCT , CM000682.1:g.3652582_3652583delinsCT	GRCh37
NC_000020.9:g.3600582_3600583delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1647_1648delinsAG MANE Select	ENSP00000348912.3:p.Gly549=
ENST00000350009.6:c.1647_1648delinsAG	ENSP00000322550.5:p.Gly549=
ENST00000356518.6:c.1647_1648delinsAG	ENSP00000348912.2:p.Gly549=
ENST00000379861.8:c.1647_1648delinsAG	ENSP00000369190.4:p.Gly549=
ENST00000466620.5:n.1286_1287delinsAG
ENST00000617732.1:c.*632-479_*632-478delinsAG	ENSP00000483343.1:n.*632-479_*632-478delinsAG
ENST00000619289.4:c.1287_1288delinsAG	ENSP00000484600.1:p.Gly429=
NM_001282447.1:c.1647_1648delinsAG	NP_001269376.1:p.Gly549=
NM_025220.3:c.1647_1648delinsAG	NP_079496.1:p.Gly549=
NM_153202.2:c.1647_1648delinsAG	NP_694882.1:p.Gly549=
XM_005260843.1:c.1686_1687delinsAG	XP_005260900.1:p.Gly562=
XM_006723639.1:c.1686_1687delinsAG	XP_006723702.1:p.Gly562=
XM_006723640.1:c.1677_1678delinsAG	XP_006723703.1:p.Gly559=
XM_011529366.1:c.1683_1684delinsAG	XP_011527668.1:p.Gly561=
XM_011529367.1:c.1644_1645delinsAG	XP_011527669.1:p.Gly548=
XM_011529368.1:c.1686_1687delinsAG	XP_011527670.1:p.Gly562=
XM_011529369.1:c.1654_1655delinsAG	XP_011527671.1:p.Arg552=
XM_011529370.1:c.1654_1655delinsAG	XP_011527672.1:p.Arg552=
XM_011529373.1:c.684_685delinsAG	XP_011527675.1:p.Gly228=
XR_937151.1:n.1790_1791delinsAG
XR_937152.1:n.1790_1791delinsAG
XR_937153.1:n.1671_1672delinsAG
XR_937154.1:n.1671_1672delinsAG
XR_937155.1:n.1592_1593delinsAG
XR_937157.1:n.1594_1595delinsAG
NM_001282447.2:c.1647_1648delinsAG	NP_001269376.1:p.Gly549=
NM_025220.4:c.1647_1648delinsAG	NP_079496.1:p.Gly549=
NM_153202.3:c.1647_1648delinsAG	NP_694882.1:p.Gly549=
XM_011529373.2:c.684_685delinsAG	XP_011527675.1:p.Gly228=
XR_001754405.1:n.1758_1759delinsAG
XR_002958534.1:n.1867_1868delinsAG
NM_001282447.3:c.1647_1648delinsAG	NP_001269376.1:p.Gly549=
NM_025220.5:c.1647_1648delinsAG MANE Select	NP_079496.1:p.Gly549=
NM_153202.4:c.1647_1648delinsAG	NP_694882.1:p.Gly549=