Canonical Allele Identifier: CA1910755771
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806611T= , CM000672.2:g.53806611T= GRCh38
NC_000010.10:g.55566371T= , CM000672.1:g.55566371T= GRCh37
NC_000010.9:g.55236377T= NCBI36
NG_009191.2:g.999681A=
NG_009191.3:g.1827572A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642496.1:c.4050A=
ENST00000644397.2:c.5191A= MANE Select ENSP00000495195.1:p.Asn1731=
ENST00000373965.6:c.5002A= ENSP00000363076.3:p.Asn1668=
ENST00000414778.5:c.4999A= ENSP00000410304.2:p.Asn1667=
ENST00000495484.5:c.1219A= ENSP00000480780.1:p.Asn407=
ENST00000614895.4:c.5014A= ENSP00000478512.1:p.Asn1672=
ENST00000616114.4:c.4996A= ENSP00000483745.1:p.Asn1666=
ENST00000618301.4:c.1351A= ENSP00000482780.1:p.Asn451=
ENST00000621708.4:c.5017A= ENSP00000484454.1:p.Asn1673=
NM_001142771.1:c.5017A= NP_001136243.1:p.Asn1673=
NM_001142772.1:c.5002A= NP_001136244.1:p.Asn1668=
NM_001354420.1:c.4996A= NP_001341349.1:p.Asn1666=
NM_001354429.1:c.5125A= NP_001341358.1:p.Asn1709=
XR_001747192.2:n.11483A=
XR_001747193.2:n.11474A=
NM_001142771.2:c.5017A= NP_001136243.1:p.Asn1673=
NM_001142772.2:c.5002A= NP_001136244.1:p.Asn1668=
NM_001354420.2:c.4996A= NP_001341349.1:p.Asn1666=
NM_001354429.2:c.5125A= NP_001341358.1:p.Asn1709=
NM_001384140.1:c.5191A= MANE Select NP_001371069.1:p.Asn1731=