Canonical Allele Identifier: CA2651725445

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3670437-A-ATGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3670439_3670440insCTG , CM000682.2:g.3670439_3670440insCTG	GRCh38
NC_000020.10:g.3651086_3651087insCTG , CM000682.1:g.3651086_3651087insCTG	GRCh37
NC_000020.9:g.3599086_3599087insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2240+568_2240+569insGCA MANE Select	ENSP00000348912.3:n.2240+568_2240+569insGCA
ENST00000350009.6:c.2162+568_2162+569insGCA	ENSP00000322550.5:n.2162+568_2162+569insGCA
ENST00000356518.6:c.2240+568_2240+569insGCA	ENSP00000348912.2:n.2240+568_2240+569insGCA
ENST00000379861.8:c.2240+568_2240+569insGCA	ENSP00000369190.4:n.2240+568_2240+569insGCA
ENST00000466620.5:n.1801+568_1801+569insGCA
ENST00000483362.1:n.188_189insGCA
ENST00000617732.1:c.*927+568_*927+569insGCA	ENSP00000483343.1:n.*927+568_*927+569insGCA
ENST00000619289.4:c.1880+568_1880+569insGCA	ENSP00000484600.1:n.1880+568_1880+569insGCA
NM_001282447.1:c.2240+568_2240+569insGCA	NP_001269376.1:n.2240+568_2240+569insGCA
NM_025220.3:c.2240+568_2240+569insGCA	NP_079496.1:n.2240+568_2240+569insGCA
NM_153202.2:c.2162+568_2162+569insGCA	NP_694882.1:n.2162+568_2162+569insGCA
XM_005260843.1:c.2279+568_2279+569insGCA	XP_005260900.1:n.2279+568_2279+569insGCA
XM_006723639.1:c.2279+568_2279+569insGCA	XP_006723702.1:n.2279+568_2279+569insGCA
XM_006723640.1:c.2270+568_2270+569insGCA	XP_006723703.1:n.2270+568_2270+569insGCA
XM_011529366.1:c.2276+568_2276+569insGCA	XP_011527668.1:n.2276+568_2276+569insGCA
XM_011529367.1:c.2237+568_2237+569insGCA	XP_011527669.1:n.2237+568_2237+569insGCA
XM_011529368.1:c.2201+568_2201+569insGCA	XP_011527670.1:n.2201+568_2201+569insGCA
XM_011529373.1:c.1277+568_1277+569insGCA	XP_011527675.1:n.1277+568_1277+569insGCA
XR_937151.1:n.2383+568_2383+569insGCA
XR_937152.1:n.2383+568_2383+569insGCA
XR_937153.1:n.2264+568_2264+569insGCA
XR_937154.1:n.2264+568_2264+569insGCA
XR_937155.1:n.2185+568_2185+569insGCA
XR_937157.1:n.2187+568_2187+569insGCA
NM_001282447.2:c.2240+568_2240+569insGCA	NP_001269376.1:n.2240+568_2240+569insGCA
NM_025220.4:c.2240+568_2240+569insGCA	NP_079496.1:n.2240+568_2240+569insGCA
NM_153202.3:c.2162+568_2162+569insGCA	NP_694882.1:n.2162+568_2162+569insGCA
XM_011529373.2:c.1277+568_1277+569insGCA	XP_011527675.1:n.1277+568_1277+569insGCA
XR_001754405.1:n.2351+568_2351+569insGCA
XR_002958534.1:n.2460+568_2460+569insGCA
NM_001282447.3:c.2240+568_2240+569insGCA	NP_001269376.1:n.2240+568_2240+569insGCA
NM_025220.5:c.2240+568_2240+569insGCA MANE Select	NP_079496.1:n.2240+568_2240+569insGCA
NM_153202.4:c.2162+568_2162+569insGCA	NP_694882.1:n.2162+568_2162+569insGCA