Canonical Allele Identifier: CA2651725028

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3670209-T-TACTTTCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3670209_3670210insACTTTCAGC , CM000682.2:g.3670209_3670210insACTTTCAGC	GRCh38
NC_000020.10:g.3650856_3650857insACTTTCAGC , CM000682.1:g.3650856_3650857insACTTTCAGC	GRCh37
NC_000020.9:g.3598856_3598857insACTTTCAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2241-573_2241-572insGCTGAAAGT MANE Select	ENSP00000348912.3:n.2241-573_2241-572insGCTGAAAGT
ENST00000350009.6:c.2163-573_2163-572insGCTGAAAGT	ENSP00000322550.5:n.2163-573_2163-572insGCTGAAAGT
ENST00000356518.6:c.2241-573_2241-572insGCTGAAAGT	ENSP00000348912.2:n.2241-573_2241-572insGCTGAAAGT
ENST00000379861.8:c.2241-573_2241-572insGCTGAAAGT	ENSP00000369190.4:n.2241-573_2241-572insGCTGAAAGT
ENST00000466620.5:n.1802-573_1802-572insGCTGAAAGT
ENST00000483362.1:n.416_417insGCTGAAAGT
ENST00000617732.1:c.*928-573_*928-572insGCTGAAAGT	ENSP00000483343.1:n.*928-573_*928-572insGCTGAAAGT
ENST00000619289.4:c.1881-573_1881-572insGCTGAAAGT	ENSP00000484600.1:n.1881-573_1881-572insGCTGAAAGT
NM_001282447.1:c.2241-573_2241-572insGCTGAAAGT	NP_001269376.1:n.2241-573_2241-572insGCTGAAAGT
NM_025220.3:c.2241-573_2241-572insGCTGAAAGT	NP_079496.1:n.2241-573_2241-572insGCTGAAAGT
NM_153202.2:c.2163-573_2163-572insGCTGAAAGT	NP_694882.1:n.2163-573_2163-572insGCTGAAAGT
XM_005260843.1:c.2280-573_2280-572insGCTGAAAGT	XP_005260900.1:n.2280-573_2280-572insGCTGAAAGT
XM_006723639.1:c.2280-573_2280-572insGCTGAAAGT	XP_006723702.1:n.2280-573_2280-572insGCTGAAAGT
XM_006723640.1:c.2271-573_2271-572insGCTGAAAGT	XP_006723703.1:n.2271-573_2271-572insGCTGAAAGT
XM_011529366.1:c.2277-573_2277-572insGCTGAAAGT	XP_011527668.1:n.2277-573_2277-572insGCTGAAAGT
XM_011529367.1:c.2238-573_2238-572insGCTGAAAGT	XP_011527669.1:n.2238-573_2238-572insGCTGAAAGT
XM_011529368.1:c.2202-573_2202-572insGCTGAAAGT	XP_011527670.1:n.2202-573_2202-572insGCTGAAAGT
XM_011529373.1:c.1278-573_1278-572insGCTGAAAGT	XP_011527675.1:n.1278-573_1278-572insGCTGAAAGT
XR_937151.1:n.2383+796_2383+797insGCTGAAAGT
XR_937152.1:n.2383+796_2383+797insGCTGAAAGT
XR_937153.1:n.2265-573_2265-572insGCTGAAAGT
XR_937154.1:n.2265-573_2265-572insGCTGAAAGT
XR_937155.1:n.2186-573_2186-572insGCTGAAAGT
XR_937157.1:n.2188-573_2188-572insGCTGAAAGT
NM_001282447.2:c.2241-573_2241-572insGCTGAAAGT	NP_001269376.1:n.2241-573_2241-572insGCTGAAAGT
NM_025220.4:c.2241-573_2241-572insGCTGAAAGT	NP_079496.1:n.2241-573_2241-572insGCTGAAAGT
NM_153202.3:c.2163-573_2163-572insGCTGAAAGT	NP_694882.1:n.2163-573_2163-572insGCTGAAAGT
XM_011529373.2:c.1278-573_1278-572insGCTGAAAGT	XP_011527675.1:n.1278-573_1278-572insGCTGAAAGT
XR_001754405.1:n.2352-573_2352-572insGCTGAAAGT
XR_002958534.1:n.2461-573_2461-572insGCTGAAAGT
NM_001282447.3:c.2241-573_2241-572insGCTGAAAGT	NP_001269376.1:n.2241-573_2241-572insGCTGAAAGT
NM_025220.5:c.2241-573_2241-572insGCTGAAAGT MANE Select	NP_079496.1:n.2241-573_2241-572insGCTGAAAGT
NM_153202.4:c.2163-573_2163-572insGCTGAAAGT	NP_694882.1:n.2163-573_2163-572insGCTGAAAGT