Canonical Allele Identifier: CA2346678862

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671795_3671796delinsAG , CM000682.2:g.3671795_3671796delinsAG	GRCh38
NC_000020.10:g.3652442_3652443delinsAG , CM000682.1:g.3652442_3652443delinsAG	GRCh37
NC_000020.9:g.3600442_3600443delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1707-17_1707-16delinsCT MANE Select	ENSP00000348912.3:n.1707-17_1707-16delinsCT
ENST00000350009.6:c.1707-17_1707-16delinsCT	ENSP00000322550.5:n.1707-17_1707-16delinsCT
ENST00000356518.6:c.1707-17_1707-16delinsCT	ENSP00000348912.2:n.1707-17_1707-16delinsCT
ENST00000379861.8:c.1707-17_1707-16delinsCT	ENSP00000369190.4:n.1707-17_1707-16delinsCT
ENST00000466620.5:n.1346-17_1346-16delinsCT
ENST00000617732.1:c.*632-339_*632-338delinsCT	ENSP00000483343.1:n.*632-339_*632-338delinsCT
ENST00000619289.4:c.1347-17_1347-16delinsCT	ENSP00000484600.1:n.1347-17_1347-16delinsCT
NM_001282447.1:c.1707-17_1707-16delinsCT	NP_001269376.1:n.1707-17_1707-16delinsCT
NM_025220.3:c.1707-17_1707-16delinsCT	NP_079496.1:n.1707-17_1707-16delinsCT
NM_153202.2:c.1707-17_1707-16delinsCT	NP_694882.1:n.1707-17_1707-16delinsCT
XM_005260843.1:c.1746-17_1746-16delinsCT	XP_005260900.1:n.1746-17_1746-16delinsCT
XM_006723639.1:c.1746-17_1746-16delinsCT	XP_006723702.1:n.1746-17_1746-16delinsCT
XM_006723640.1:c.1737-17_1737-16delinsCT	XP_006723703.1:n.1737-17_1737-16delinsCT
XM_011529366.1:c.1743-17_1743-16delinsCT	XP_011527668.1:n.1743-17_1743-16delinsCT
XM_011529367.1:c.1704-17_1704-16delinsCT	XP_011527669.1:n.1704-17_1704-16delinsCT
XM_011529368.1:c.1746-17_1746-16delinsCT	XP_011527670.1:n.1746-17_1746-16delinsCT
XM_011529369.1:c.1714-17_1714-16delinsCT	XP_011527671.1:n.1714-17_1714-16delinsCT
XM_011529370.1:c.1714-17_1714-16delinsCT	XP_011527672.1:n.1714-17_1714-16delinsCT
XM_011529373.1:c.744-17_744-16delinsCT	XP_011527675.1:n.744-17_744-16delinsCT
XR_937151.1:n.1850-17_1850-16delinsCT
XR_937152.1:n.1850-17_1850-16delinsCT
XR_937153.1:n.1731-17_1731-16delinsCT
XR_937154.1:n.1731-17_1731-16delinsCT
XR_937155.1:n.1652-17_1652-16delinsCT
XR_937157.1:n.1654-17_1654-16delinsCT
NM_001282447.2:c.1707-17_1707-16delinsCT	NP_001269376.1:n.1707-17_1707-16delinsCT
NM_025220.4:c.1707-17_1707-16delinsCT	NP_079496.1:n.1707-17_1707-16delinsCT
NM_153202.3:c.1707-17_1707-16delinsCT	NP_694882.1:n.1707-17_1707-16delinsCT
XM_011529373.2:c.744-17_744-16delinsCT	XP_011527675.1:n.744-17_744-16delinsCT
XR_001754405.1:n.1818-17_1818-16delinsCT
XR_002958534.1:n.1927-17_1927-16delinsCT
NM_001282447.3:c.1707-17_1707-16delinsCT	NP_001269376.1:n.1707-17_1707-16delinsCT
NM_025220.5:c.1707-17_1707-16delinsCT MANE Select	NP_079496.1:n.1707-17_1707-16delinsCT
NM_153202.4:c.1707-17_1707-16delinsCT	NP_694882.1:n.1707-17_1707-16delinsCT