Canonical Allele Identifier: CA2346677711
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669604_3669605delinsCA , CM000682.2:g.3669604_3669605delinsCA GRCh38
NC_000020.10:g.3650251_3650252delinsCA , CM000682.1:g.3650251_3650252delinsCA GRCh37
NC_000020.9:g.3598251_3598252delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2273_2274delinsTG MANE Select ENSP00000348912.3:p.Leu758=
ENST00000350009.6:c.2195_2196delinsTG ENSP00000322550.5:p.Leu732=
ENST00000356518.6:c.2273_2274delinsTG ENSP00000348912.2:p.Leu758=
ENST00000379861.8:c.2273_2274delinsTG ENSP00000369190.4:p.Leu758=
ENST00000466620.5:n.1834_1835delinsTG
ENST00000483362.1:n.1021_1022delinsTG
ENST00000617732.1:c.*960_*961delinsTG ENSP00000483343.1:n.*960_*961delinsTG
ENST00000619289.4:c.1913_1914delinsTG ENSP00000484600.1:p.Leu638=
NM_001282447.1:c.2273_2274delinsTG NP_001269376.1:p.Leu758=
NM_025220.3:c.2273_2274delinsTG NP_079496.1:p.Leu758=
NM_153202.2:c.2195_2196delinsTG NP_694882.1:p.Leu732=
XM_005260843.1:c.2312_2313delinsTG XP_005260900.1:p.Leu771=
XM_006723639.1:c.2312_2313delinsTG XP_006723702.1:p.Leu771=
XM_006723640.1:c.2303_2304delinsTG XP_006723703.1:p.Leu768=
XM_011529366.1:c.2309_2310delinsTG XP_011527668.1:p.Leu770=
XM_011529367.1:c.2270_2271delinsTG XP_011527669.1:p.Leu757=
XM_011529368.1:c.2234_2235delinsTG XP_011527670.1:p.Leu745=
XM_011529373.1:c.1310_1311delinsTG XP_011527675.1:p.Leu437=
XR_937151.1:n.2384-235_2384-234delinsTG
XR_937152.1:n.2384-235_2384-234delinsTG
XR_937153.1:n.2297_2298delinsTG
XR_937154.1:n.2297_2298delinsTG
XR_937155.1:n.2218_2219delinsTG
XR_937157.1:n.2220_2221delinsTG
NM_001282447.2:c.2273_2274delinsTG NP_001269376.1:p.Leu758=
NM_025220.4:c.2273_2274delinsTG NP_079496.1:p.Leu758=
NM_153202.3:c.2195_2196delinsTG NP_694882.1:p.Leu732=
XM_011529373.2:c.1310_1311delinsTG XP_011527675.1:p.Leu437=
XR_001754405.1:n.2384_2385delinsTG
XR_002958534.1:n.2493_2494delinsTG
NM_001282447.3:c.2273_2274delinsTG NP_001269376.1:p.Leu758=
NM_025220.5:c.2273_2274delinsTG MANE Select NP_079496.1:p.Leu758=
NM_153202.4:c.2195_2196delinsTG NP_694882.1:p.Leu732=