Canonical Allele Identifier: CA1910763249
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53809370_53809371delinsTC , CM000672.2:g.53809370_53809371delinsTC GRCh38
NC_000010.10:g.55569130_55569131delinsTC , CM000672.1:g.55569130_55569131delinsTC GRCh37
NC_000010.9:g.55239136_55239137delinsTC NCBI36
NG_009191.2:g.996921_996922delinsGA
NG_009191.3:g.1824812_1824813delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000613657.6:c.4694_4695delinsGA ENSP00000482794.1:p.Arg1565=
ENST00000395445.6:c.4673_4674delinsGA ENSP00000378832.2:p.Arg1558=
ENST00000613657.5:c.4694_4695delinsGA ENSP00000482794.1:p.Arg1565=
ENST00000642496.1:c.3530+1185_3530+1186delinsGA
ENST00000644397.2:c.4671+1185_4671+1186delinsGA MANE Select ENSP00000495195.1:n.4671+1185_4671+1186delinsGA
ENST00000373965.6:c.4482+1185_4482+1186delinsGA ENSP00000363076.3:n.4482+1185_4482+1186delinsGA
ENST00000395438.5:c.*109_*110delinsGA ENSP00000378826.2:n.*109_*110delinsGA
ENST00000395440.5:c.1481_1482delinsGA ENSP00000378827.1:p.Arg494=
ENST00000395442.5:c.1274_1275delinsGA ENSP00000378829.1:p.Arg425=
ENST00000395445.5:c.4673_4674delinsGA ENSP00000378832.2:p.Arg1558=
ENST00000395446.5:c.2267_2268delinsGA ENSP00000378833.1:p.Arg756=
ENST00000409834.5:c.*109_*110delinsGA ENSP00000386693.1:n.*109_*110delinsGA
ENST00000414367.5:c.*732_*733delinsGA ENSP00000412531.1:n.*732_*733delinsGA
ENST00000414778.5:c.4479+1185_4479+1186delinsGA ENSP00000410304.2:n.4479+1185_4479+1186delinsGA
ENST00000476074.5:n.609+1185_609+1186delinsGA
ENST00000495484.5:c.699+1185_699+1186delinsGA ENSP00000480780.1:n.699+1185_699+1186delinsGA
ENST00000612394.4:c.4691_4692delinsGA ENSP00000482921.1:p.Arg1564=
ENST00000613657.4:c.4694_4695delinsGA ENSP00000482794.1:p.Arg1565=
ENST00000614895.4:c.4494+1185_4494+1186delinsGA ENSP00000478512.1:n.4494+1185_4494+1186delinsGA
ENST00000615043.1:c.294_295delinsGA
ENST00000616114.4:c.4476+1185_4476+1186delinsGA ENSP00000483745.1:n.4476+1185_4476+1186delinsGA
ENST00000617271.4:c.*109_*110delinsGA ENSP00000478076.1:n.*109_*110delinsGA
ENST00000618301.4:c.831+1185_831+1186delinsGA ENSP00000482780.1:n.831+1185_831+1186delinsGA
ENST00000621708.4:c.4497+1185_4497+1186delinsGA ENSP00000484454.1:n.4497+1185_4497+1186delinsGA
NM_001142769.1:c.4694_4695delinsGA NP_001136241.1:p.Arg1565=
NM_001142770.1:c.*109_*110delinsGA NP_001136242.1:n.*109_*110delinsGA
NM_001142771.1:c.4497+1185_4497+1186delinsGA NP_001136243.1:n.4497+1185_4497+1186delinsGA
NM_001142772.1:c.4482+1185_4482+1186delinsGA NP_001136244.1:n.4482+1185_4482+1186delinsGA
NM_001142769.2:c.4694_4695delinsGA NP_001136241.1:p.Arg1565=
NM_001142770.2:c.*109_*110delinsGA NP_001136242.1:n.*109_*110delinsGA
NM_001354411.1:c.4673_4674delinsGA NP_001341340.1:p.Arg1558=
NM_001354420.1:c.4476+1185_4476+1186delinsGA NP_001341349.1:n.4476+1185_4476+1186delinsGA
NM_001354429.1:c.4605+1185_4605+1186delinsGA NP_001341358.1:n.4605+1185_4605+1186delinsGA
XM_017016573.2:c.4673_4674delinsGA XP_016872062.1:p.Arg1558=
XR_001747192.2:n.10963+1185_10963+1186delinsGA
XR_001747193.2:n.10954+1185_10954+1186delinsGA
NM_001142769.3:c.4694_4695delinsGA NP_001136241.1:p.Arg1565=
NM_001142770.3:c.*109_*110delinsGA NP_001136242.1:n.*109_*110delinsGA
NM_001142771.2:c.4497+1185_4497+1186delinsGA NP_001136243.1:n.4497+1185_4497+1186delinsGA
NM_001142772.2:c.4482+1185_4482+1186delinsGA NP_001136244.1:n.4482+1185_4482+1186delinsGA
NM_001354411.2:c.4673_4674delinsGA NP_001341340.1:p.Arg1558=
NM_001354420.2:c.4476+1185_4476+1186delinsGA NP_001341349.1:n.4476+1185_4476+1186delinsGA
NM_001354429.2:c.4605+1185_4605+1186delinsGA NP_001341358.1:n.4605+1185_4605+1186delinsGA
NM_001384140.1:c.4671+1185_4671+1186delinsGA MANE Select NP_001371069.1:n.4671+1185_4671+1186delinsGA