Canonical Allele Identifier: CA469545859

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566474A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806714A>C , CM000672.2:g.53806714A>C	GRCh38
NC_000010.10:g.55566474A>C , CM000672.1:g.55566474A>C	GRCh37
NC_000010.9:g.55236480A>C	NCBI36
NG_009191.2:g.999578T>G
NG_009191.3:g.1827469T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.3947T>G
ENST00000644397.2:c.5088T>G MANE Select	ENSP00000495195.1:p.Val1696=
ENST00000373965.6:c.4899T>G	ENSP00000363076.3:p.Val1633=
ENST00000414778.5:c.4896T>G	ENSP00000410304.2:p.Val1632=
ENST00000495484.5:c.1116T>G	ENSP00000480780.1:p.Val372=
ENST00000614895.4:c.4911T>G	ENSP00000478512.1:p.Val1637=
ENST00000616114.4:c.4893T>G	ENSP00000483745.1:p.Val1631=
ENST00000618301.4:c.1248T>G	ENSP00000482780.1:p.Val416=
ENST00000621708.4:c.4914T>G	ENSP00000484454.1:p.Val1638=
NM_001142771.1:c.4914T>G	NP_001136243.1:p.Val1638=
NM_001142772.1:c.4899T>G	NP_001136244.1:p.Val1633=
NM_001354420.1:c.4893T>G	NP_001341349.1:p.Val1631=
NM_001354429.1:c.5022T>G	NP_001341358.1:p.Val1674=
XR_001747192.2:n.11380T>G
XR_001747193.2:n.11371T>G
NM_001142771.2:c.4914T>G	NP_001136243.1:p.Val1638=
NM_001142772.2:c.4899T>G	NP_001136244.1:p.Val1633=
NM_001354420.2:c.4893T>G	NP_001341349.1:p.Val1631=
NM_001354429.2:c.5022T>G	NP_001341358.1:p.Val1674=
NM_001384140.1:c.5088T>G MANE Select	NP_001371069.1:p.Val1696=