Canonical Allele Identifier: CA469545905

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566540G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806780G>T , CM000672.2:g.53806780G>T	GRCh38
NC_000010.10:g.55566540G>T , CM000672.1:g.55566540G>T	GRCh37
NC_000010.9:g.55236546G>T	NCBI36
NG_009191.2:g.999512C>A
NG_009191.3:g.1827403C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3881C>A
ENST00000644397.2:c.5022C>A MANE Select	ENSP00000495195.1:p.Ala1674=
ENST00000373965.6:c.4833C>A	ENSP00000363076.3:p.Ala1611=
ENST00000414778.5:c.4830C>A	ENSP00000410304.2:p.Ala1610=
ENST00000495484.5:c.1050C>A	ENSP00000480780.1:p.Ala350=
ENST00000614895.4:c.4845C>A	ENSP00000478512.1:p.Ala1615=
ENST00000616114.4:c.4827C>A	ENSP00000483745.1:p.Ala1609=
ENST00000618301.4:c.1182C>A	ENSP00000482780.1:p.Ala394=
ENST00000621708.4:c.4848C>A	ENSP00000484454.1:p.Ala1616=
NM_001142771.1:c.4848C>A	NP_001136243.1:p.Ala1616=
NM_001142772.1:c.4833C>A	NP_001136244.1:p.Ala1611=
NM_001354420.1:c.4827C>A	NP_001341349.1:p.Ala1609=
NM_001354429.1:c.4956C>A	NP_001341358.1:p.Ala1652=
XR_001747192.2:n.11314C>A
XR_001747193.2:n.11305C>A
NM_001142771.2:c.4848C>A	NP_001136243.1:p.Ala1616=
NM_001142772.2:c.4833C>A	NP_001136244.1:p.Ala1611=
NM_001354420.2:c.4827C>A	NP_001341349.1:p.Ala1609=
NM_001354429.2:c.4956C>A	NP_001341358.1:p.Ala1652=
NM_001384140.1:c.5022C>A MANE Select	NP_001371069.1:p.Ala1674=