Canonical Allele Identifier: CA1910763302
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53809399_53809400delinsTA , CM000672.2:g.53809399_53809400delinsTA GRCh38
NC_000010.10:g.55569159_55569160delinsTA , CM000672.1:g.55569159_55569160delinsTA GRCh37
NC_000010.9:g.55239165_55239166delinsTA NCBI36
NG_009191.2:g.996892_996893delinsTA
NG_009191.3:g.1824783_1824784delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000613657.6:c.4665_4666delinsTA ENSP00000482794.1:p.Phe1555=
ENST00000395445.6:c.4644_4645delinsTA ENSP00000378832.2:p.Phe1548=
ENST00000613657.5:c.4665_4666delinsTA ENSP00000482794.1:p.Phe1555=
ENST00000642496.1:c.3530+1156_3530+1157delinsTA
ENST00000644397.2:c.4671+1156_4671+1157delinsTA MANE Select ENSP00000495195.1:n.4671+1156_4671+1157delinsTA
ENST00000373965.6:c.4482+1156_4482+1157delinsTA ENSP00000363076.3:n.4482+1156_4482+1157delinsTA
ENST00000395438.5:c.*80_*81delinsTA ENSP00000378826.2:n.*80_*81delinsTA
ENST00000395440.5:c.1452_1453delinsTA ENSP00000378827.1:p.Phe484=
ENST00000395442.5:c.1245_1246delinsTA ENSP00000378829.1:p.Phe415=
ENST00000395445.5:c.4644_4645delinsTA ENSP00000378832.2:p.Phe1548=
ENST00000395446.5:c.2238_2239delinsTA ENSP00000378833.1:p.Phe746=
ENST00000409834.5:c.*80_*81delinsTA ENSP00000386693.1:n.*80_*81delinsTA
ENST00000414367.5:c.*703_*704delinsTA ENSP00000412531.1:n.*703_*704delinsTA
ENST00000414778.5:c.4479+1156_4479+1157delinsTA ENSP00000410304.2:n.4479+1156_4479+1157delinsTA
ENST00000476074.5:n.609+1156_609+1157delinsTA
ENST00000495484.5:c.699+1156_699+1157delinsTA ENSP00000480780.1:n.699+1156_699+1157delinsTA
ENST00000612394.4:c.4662_4663delinsTA ENSP00000482921.1:p.Phe1554=
ENST00000613657.4:c.4665_4666delinsTA ENSP00000482794.1:p.Phe1555=
ENST00000614895.4:c.4494+1156_4494+1157delinsTA ENSP00000478512.1:n.4494+1156_4494+1157delinsTA
ENST00000615043.1:c.265_266delinsTA
ENST00000616114.4:c.4476+1156_4476+1157delinsTA ENSP00000483745.1:n.4476+1156_4476+1157delinsTA
ENST00000617271.4:c.*80_*81delinsTA ENSP00000478076.1:n.*80_*81delinsTA
ENST00000618301.4:c.831+1156_831+1157delinsTA ENSP00000482780.1:n.831+1156_831+1157delinsTA
ENST00000621708.4:c.4497+1156_4497+1157delinsTA ENSP00000484454.1:n.4497+1156_4497+1157delinsTA
NM_001142769.1:c.4665_4666delinsTA NP_001136241.1:p.Phe1555=
NM_001142770.1:c.*80_*81delinsTA NP_001136242.1:n.*80_*81delinsTA
NM_001142771.1:c.4497+1156_4497+1157delinsTA NP_001136243.1:n.4497+1156_4497+1157delinsTA
NM_001142772.1:c.4482+1156_4482+1157delinsTA NP_001136244.1:n.4482+1156_4482+1157delinsTA
NM_001142769.2:c.4665_4666delinsTA NP_001136241.1:p.Phe1555=
NM_001142770.2:c.*80_*81delinsTA NP_001136242.1:n.*80_*81delinsTA
NM_001354411.1:c.4644_4645delinsTA NP_001341340.1:p.Phe1548=
NM_001354420.1:c.4476+1156_4476+1157delinsTA NP_001341349.1:n.4476+1156_4476+1157delinsTA
NM_001354429.1:c.4605+1156_4605+1157delinsTA NP_001341358.1:n.4605+1156_4605+1157delinsTA
XM_017016573.2:c.4644_4645delinsTA XP_016872062.1:p.Phe1548=
XR_001747192.2:n.10963+1156_10963+1157delinsTA
XR_001747193.2:n.10954+1156_10954+1157delinsTA
NM_001142769.3:c.4665_4666delinsTA NP_001136241.1:p.Phe1555=
NM_001142770.3:c.*80_*81delinsTA NP_001136242.1:n.*80_*81delinsTA
NM_001142771.2:c.4497+1156_4497+1157delinsTA NP_001136243.1:n.4497+1156_4497+1157delinsTA
NM_001142772.2:c.4482+1156_4482+1157delinsTA NP_001136244.1:n.4482+1156_4482+1157delinsTA
NM_001354411.2:c.4644_4645delinsTA NP_001341340.1:p.Phe1548=
NM_001354420.2:c.4476+1156_4476+1157delinsTA NP_001341349.1:n.4476+1156_4476+1157delinsTA
NM_001354429.2:c.4605+1156_4605+1157delinsTA NP_001341358.1:n.4605+1156_4605+1157delinsTA
NM_001384140.1:c.4671+1156_4671+1157delinsTA MANE Select NP_001371069.1:n.4671+1156_4671+1157delinsTA