Canonical Allele Identifier: CA1910756034
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806707C= , CM000672.2:g.53806707C= GRCh38
NC_000010.10:g.55566467C= , CM000672.1:g.55566467C= GRCh37
NC_000010.9:g.55236473C= NCBI36
NG_009191.2:g.999585G=
NG_009191.3:g.1827476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642496.1:c.3954G=
ENST00000644397.2:c.5095G= MANE Select ENSP00000495195.1:p.Glu1699=
ENST00000373965.6:c.4906G= ENSP00000363076.3:p.Glu1636=
ENST00000414778.5:c.4903G= ENSP00000410304.2:p.Glu1635=
ENST00000495484.5:c.1123G= ENSP00000480780.1:p.Glu375=
ENST00000614895.4:c.4918G= ENSP00000478512.1:p.Glu1640=
ENST00000616114.4:c.4900G= ENSP00000483745.1:p.Glu1634=
ENST00000618301.4:c.1255G= ENSP00000482780.1:p.Glu419=
ENST00000621708.4:c.4921G= ENSP00000484454.1:p.Glu1641=
NM_001142771.1:c.4921G= NP_001136243.1:p.Glu1641=
NM_001142772.1:c.4906G= NP_001136244.1:p.Glu1636=
NM_001354420.1:c.4900G= NP_001341349.1:p.Glu1634=
NM_001354429.1:c.5029G= NP_001341358.1:p.Glu1677=
XR_001747192.2:n.11387G=
XR_001747193.2:n.11378G=
NM_001142771.2:c.4921G= NP_001136243.1:p.Glu1641=
NM_001142772.2:c.4906G= NP_001136244.1:p.Glu1636=
NM_001354420.2:c.4900G= NP_001341349.1:p.Glu1634=
NM_001354429.2:c.5029G= NP_001341358.1:p.Glu1677=
NM_001384140.1:c.5095G= MANE Select NP_001371069.1:p.Glu1699=