Canonical Allele Identifier: CA2651726207

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3670744-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3670748_3670749del , CM000682.2:g.3670748_3670749del	GRCh38
NC_000020.10:g.3651395_3651396del , CM000682.1:g.3651395_3651396del	GRCh37
NC_000020.9:g.3599395_3599396del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2240+260_2240+261del MANE Select	ENSP00000348912.3:n.2240+260_2240+261del
ENST00000350009.6:c.2162+260_2162+261del	ENSP00000322550.5:n.2162+260_2162+261del
ENST00000356518.6:c.2240+260_2240+261del	ENSP00000348912.2:n.2240+260_2240+261del
ENST00000379861.8:c.2240+260_2240+261del	ENSP00000369190.4:n.2240+260_2240+261del
ENST00000466620.5:n.1801+260_1801+261del
ENST00000617732.1:c.*927+260_*927+261del	ENSP00000483343.1:n.*927+260_*927+261del
ENST00000619289.4:c.1880+260_1880+261del	ENSP00000484600.1:n.1880+260_1880+261del
NM_001282447.1:c.2240+260_2240+261del	NP_001269376.1:n.2240+260_2240+261del
NM_025220.3:c.2240+260_2240+261del	NP_079496.1:n.2240+260_2240+261del
NM_153202.2:c.2162+260_2162+261del	NP_694882.1:n.2162+260_2162+261del
XM_005260843.1:c.2279+260_2279+261del	XP_005260900.1:n.2279+260_2279+261del
XM_006723639.1:c.2279+260_2279+261del	XP_006723702.1:n.2279+260_2279+261del
XM_006723640.1:c.2270+260_2270+261del	XP_006723703.1:n.2270+260_2270+261del
XM_011529366.1:c.2276+260_2276+261del	XP_011527668.1:n.2276+260_2276+261del
XM_011529367.1:c.2237+260_2237+261del	XP_011527669.1:n.2237+260_2237+261del
XM_011529368.1:c.2201+260_2201+261del	XP_011527670.1:n.2201+260_2201+261del
XM_011529373.1:c.1277+260_1277+261del	XP_011527675.1:n.1277+260_1277+261del
XR_937151.1:n.2383+260_2383+261del
XR_937152.1:n.2383+260_2383+261del
XR_937153.1:n.2264+260_2264+261del
XR_937154.1:n.2264+260_2264+261del
XR_937155.1:n.2185+260_2185+261del
XR_937157.1:n.2187+260_2187+261del
NM_001282447.2:c.2240+260_2240+261del	NP_001269376.1:n.2240+260_2240+261del
NM_025220.4:c.2240+260_2240+261del	NP_079496.1:n.2240+260_2240+261del
NM_153202.3:c.2162+260_2162+261del	NP_694882.1:n.2162+260_2162+261del
XM_011529373.2:c.1277+260_1277+261del	XP_011527675.1:n.1277+260_1277+261del
XR_001754405.1:n.2351+260_2351+261del
XR_002958534.1:n.2460+260_2460+261del
NM_001282447.3:c.2240+260_2240+261del	NP_001269376.1:n.2240+260_2240+261del
NM_025220.5:c.2240+260_2240+261del MANE Select	NP_079496.1:n.2240+260_2240+261del
NM_153202.4:c.2162+260_2162+261del	NP_694882.1:n.2162+260_2162+261del