Canonical Allele Identifier: CA1910756031
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806704A= , CM000672.2:g.53806704A= GRCh38
NC_000010.10:g.55566464A= , CM000672.1:g.55566464A= GRCh37
NC_000010.9:g.55236470A= NCBI36
NG_009191.2:g.999588T=
NG_009191.3:g.1827479T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642496.1:c.3957T=
ENST00000644397.2:c.5098T= MANE Select ENSP00000495195.1:p.Ser1700=
ENST00000373965.6:c.4909T= ENSP00000363076.3:p.Ser1637=
ENST00000414778.5:c.4906T= ENSP00000410304.2:p.Ser1636=
ENST00000495484.5:c.1126T= ENSP00000480780.1:p.Ser376=
ENST00000614895.4:c.4921T= ENSP00000478512.1:p.Ser1641=
ENST00000616114.4:c.4903T= ENSP00000483745.1:p.Ser1635=
ENST00000618301.4:c.1258T= ENSP00000482780.1:p.Ser420=
ENST00000621708.4:c.4924T= ENSP00000484454.1:p.Ser1642=
NM_001142771.1:c.4924T= NP_001136243.1:p.Ser1642=
NM_001142772.1:c.4909T= NP_001136244.1:p.Ser1637=
NM_001354420.1:c.4903T= NP_001341349.1:p.Ser1635=
NM_001354429.1:c.5032T= NP_001341358.1:p.Ser1678=
XR_001747192.2:n.11390T=
XR_001747193.2:n.11381T=
NM_001142771.2:c.4924T= NP_001136243.1:p.Ser1642=
NM_001142772.2:c.4909T= NP_001136244.1:p.Ser1637=
NM_001354420.2:c.4903T= NP_001341349.1:p.Ser1635=
NM_001354429.2:c.5032T= NP_001341358.1:p.Ser1678=
NM_001384140.1:c.5098T= MANE Select NP_001371069.1:p.Ser1700=