Canonical Allele Identifier: CA469545838

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566423A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806663A>G , CM000672.2:g.53806663A>G	GRCh38
NC_000010.10:g.55566423A>G , CM000672.1:g.55566423A>G	GRCh37
NC_000010.9:g.55236429A>G	NCBI36
NG_009191.2:g.999629T>C
NG_009191.3:g.1827520T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3998T>C
ENST00000644397.2:c.5139T>C MANE Select	ENSP00000495195.1:p.Phe1713=
ENST00000373965.6:c.4950T>C	ENSP00000363076.3:p.Phe1650=
ENST00000414778.5:c.4947T>C	ENSP00000410304.2:p.Phe1649=
ENST00000495484.5:c.1167T>C	ENSP00000480780.1:p.Phe389=
ENST00000614895.4:c.4962T>C	ENSP00000478512.1:p.Phe1654=
ENST00000616114.4:c.4944T>C	ENSP00000483745.1:p.Phe1648=
ENST00000618301.4:c.1299T>C	ENSP00000482780.1:p.Phe433=
ENST00000621708.4:c.4965T>C	ENSP00000484454.1:p.Phe1655=
NM_001142771.1:c.4965T>C	NP_001136243.1:p.Phe1655=
NM_001142772.1:c.4950T>C	NP_001136244.1:p.Phe1650=
NM_001354420.1:c.4944T>C	NP_001341349.1:p.Phe1648=
NM_001354429.1:c.5073T>C	NP_001341358.1:p.Phe1691=
XR_001747192.2:n.11431T>C
XR_001747193.2:n.11422T>C
NM_001142771.2:c.4965T>C	NP_001136243.1:p.Phe1655=
NM_001142772.2:c.4950T>C	NP_001136244.1:p.Phe1650=
NM_001354420.2:c.4944T>C	NP_001341349.1:p.Phe1648=
NM_001354429.2:c.5073T>C	NP_001341358.1:p.Phe1691=
NM_001384140.1:c.5139T>C MANE Select	NP_001371069.1:p.Phe1713=