Canonical Allele Identifier: CA469545856

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566465C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806705C>T , CM000672.2:g.53806705C>T	GRCh38
NC_000010.10:g.55566465C>T , CM000672.1:g.55566465C>T	GRCh37
NC_000010.9:g.55236471C>T	NCBI36
NG_009191.2:g.999587G>A
NG_009191.3:g.1827478G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.3956G>A
ENST00000644397.2:c.5097G>A MANE Select	ENSP00000495195.1:p.Glu1699=
ENST00000373965.6:c.4908G>A	ENSP00000363076.3:p.Glu1636=
ENST00000414778.5:c.4905G>A	ENSP00000410304.2:p.Glu1635=
ENST00000495484.5:c.1125G>A	ENSP00000480780.1:p.Glu375=
ENST00000614895.4:c.4920G>A	ENSP00000478512.1:p.Glu1640=
ENST00000616114.4:c.4902G>A	ENSP00000483745.1:p.Glu1634=
ENST00000618301.4:c.1257G>A	ENSP00000482780.1:p.Glu419=
ENST00000621708.4:c.4923G>A	ENSP00000484454.1:p.Glu1641=
NM_001142771.1:c.4923G>A	NP_001136243.1:p.Glu1641=
NM_001142772.1:c.4908G>A	NP_001136244.1:p.Glu1636=
NM_001354420.1:c.4902G>A	NP_001341349.1:p.Glu1634=
NM_001354429.1:c.5031G>A	NP_001341358.1:p.Glu1677=
XR_001747192.2:n.11389G>A
XR_001747193.2:n.11380G>A
NM_001142771.2:c.4923G>A	NP_001136243.1:p.Glu1641=
NM_001142772.2:c.4908G>A	NP_001136244.1:p.Glu1636=
NM_001354420.2:c.4902G>A	NP_001341349.1:p.Glu1634=
NM_001354429.2:c.5031G>A	NP_001341358.1:p.Glu1677=
NM_001384140.1:c.5097G>A MANE Select	NP_001371069.1:p.Glu1699=