Canonical Allele Identifier: CA1910755744
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806605G= , CM000672.2:g.53806605G= GRCh38
NC_000010.10:g.55566365G= , CM000672.1:g.55566365G= GRCh37
NC_000010.9:g.55236371G= NCBI36
NG_009191.2:g.999687C=
NG_009191.3:g.1827578C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642496.1:c.4056C=
ENST00000644397.2:c.5197C= MANE Select ENSP00000495195.1:p.Leu1733=
ENST00000373965.6:c.5008C= ENSP00000363076.3:p.Leu1670=
ENST00000414778.5:c.5005C= ENSP00000410304.2:p.Leu1669=
ENST00000495484.5:c.1225C= ENSP00000480780.1:p.Leu409=
ENST00000614895.4:c.5020C= ENSP00000478512.1:p.Leu1674=
ENST00000616114.4:c.5002C= ENSP00000483745.1:p.Leu1668=
ENST00000618301.4:c.1357C= ENSP00000482780.1:p.Leu453=
ENST00000621708.4:c.5023C= ENSP00000484454.1:p.Leu1675=
NM_001142771.1:c.5023C= NP_001136243.1:p.Leu1675=
NM_001142772.1:c.5008C= NP_001136244.1:p.Leu1670=
NM_001354420.1:c.5002C= NP_001341349.1:p.Leu1668=
NM_001354429.1:c.5131C= NP_001341358.1:p.Leu1711=
XR_001747192.2:n.11489C=
XR_001747193.2:n.11480C=
NM_001142771.2:c.5023C= NP_001136243.1:p.Leu1675=
NM_001142772.2:c.5008C= NP_001136244.1:p.Leu1670=
NM_001354420.2:c.5002C= NP_001341349.1:p.Leu1668=
NM_001354429.2:c.5131C= NP_001341358.1:p.Leu1711=
NM_001384140.1:c.5197C= MANE Select NP_001371069.1:p.Leu1733=