Canonical Allele Identifier: CA1910756046
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806710G= , CM000672.2:g.53806710G= GRCh38
NC_000010.10:g.55566470G= , CM000672.1:g.55566470G= GRCh37
NC_000010.9:g.55236476G= NCBI36
NG_009191.2:g.999582C=
NG_009191.3:g.1827473C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642496.1:c.3951C=
ENST00000644397.2:c.5092C= MANE Select ENSP00000495195.1:p.Gln1698=
ENST00000373965.6:c.4903C= ENSP00000363076.3:p.Gln1635=
ENST00000414778.5:c.4900C= ENSP00000410304.2:p.Gln1634=
ENST00000495484.5:c.1120C= ENSP00000480780.1:p.Gln374=
ENST00000614895.4:c.4915C= ENSP00000478512.1:p.Gln1639=
ENST00000616114.4:c.4897C= ENSP00000483745.1:p.Gln1633=
ENST00000618301.4:c.1252C= ENSP00000482780.1:p.Gln418=
ENST00000621708.4:c.4918C= ENSP00000484454.1:p.Gln1640=
NM_001142771.1:c.4918C= NP_001136243.1:p.Gln1640=
NM_001142772.1:c.4903C= NP_001136244.1:p.Gln1635=
NM_001354420.1:c.4897C= NP_001341349.1:p.Gln1633=
NM_001354429.1:c.5026C= NP_001341358.1:p.Gln1676=
XR_001747192.2:n.11384C=
XR_001747193.2:n.11375C=
NM_001142771.2:c.4918C= NP_001136243.1:p.Gln1640=
NM_001142772.2:c.4903C= NP_001136244.1:p.Gln1635=
NM_001354420.2:c.4897C= NP_001341349.1:p.Gln1633=
NM_001354429.2:c.5026C= NP_001341358.1:p.Gln1676=
NM_001384140.1:c.5092C= MANE Select NP_001371069.1:p.Gln1698=