Canonical Allele Identifier: CA2346677713
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669605_3669606delinsAG , CM000682.2:g.3669605_3669606delinsAG GRCh38
NC_000020.10:g.3650252_3650253delinsAG , CM000682.1:g.3650252_3650253delinsAG GRCh37
NC_000020.9:g.3598252_3598253delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2272_2273delinsCT MANE Select ENSP00000348912.3:p.Leu758=
ENST00000350009.6:c.2194_2195delinsCT ENSP00000322550.5:p.Leu732=
ENST00000356518.6:c.2272_2273delinsCT ENSP00000348912.2:p.Leu758=
ENST00000379861.8:c.2272_2273delinsCT ENSP00000369190.4:p.Leu758=
ENST00000466620.5:n.1833_1834delinsCT
ENST00000483362.1:n.1020_1021delinsCT
ENST00000617732.1:c.*959_*960delinsCT ENSP00000483343.1:n.*959_*960delinsCT
ENST00000619289.4:c.1912_1913delinsCT ENSP00000484600.1:p.Leu638=
NM_001282447.1:c.2272_2273delinsCT NP_001269376.1:p.Leu758=
NM_025220.3:c.2272_2273delinsCT NP_079496.1:p.Leu758=
NM_153202.2:c.2194_2195delinsCT NP_694882.1:p.Leu732=
XM_005260843.1:c.2311_2312delinsCT XP_005260900.1:p.Leu771=
XM_006723639.1:c.2311_2312delinsCT XP_006723702.1:p.Leu771=
XM_006723640.1:c.2302_2303delinsCT XP_006723703.1:p.Leu768=
XM_011529366.1:c.2308_2309delinsCT XP_011527668.1:p.Leu770=
XM_011529367.1:c.2269_2270delinsCT XP_011527669.1:p.Leu757=
XM_011529368.1:c.2233_2234delinsCT XP_011527670.1:p.Leu745=
XM_011529373.1:c.1309_1310delinsCT XP_011527675.1:p.Leu437=
XR_937151.1:n.2384-236_2384-235delinsCT
XR_937152.1:n.2384-236_2384-235delinsCT
XR_937153.1:n.2296_2297delinsCT
XR_937154.1:n.2296_2297delinsCT
XR_937155.1:n.2217_2218delinsCT
XR_937157.1:n.2219_2220delinsCT
NM_001282447.2:c.2272_2273delinsCT NP_001269376.1:p.Leu758=
NM_025220.4:c.2272_2273delinsCT NP_079496.1:p.Leu758=
NM_153202.3:c.2194_2195delinsCT NP_694882.1:p.Leu732=
XM_011529373.2:c.1309_1310delinsCT XP_011527675.1:p.Leu437=
XR_001754405.1:n.2383_2384delinsCT
XR_002958534.1:n.2492_2493delinsCT
NM_001282447.3:c.2272_2273delinsCT NP_001269376.1:p.Leu758=
NM_025220.5:c.2272_2273delinsCT MANE Select NP_079496.1:p.Leu758=
NM_153202.4:c.2194_2195delinsCT NP_694882.1:p.Leu732=