Canonical Allele Identifier: CA469545853

Gene: PCDH15

Linked Data

• gnomAD v4: 10-53806702-G-A
• MyVariant Identifiers: chr10:g.55566462G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806702G>A , CM000672.2:g.53806702G>A	GRCh38
NC_000010.10:g.55566462G>A , CM000672.1:g.55566462G>A	GRCh37
NC_000010.9:g.55236468G>A	NCBI36
NG_009191.2:g.999590C>T
NG_009191.3:g.1827481C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.3959C>T
ENST00000644397.2:c.5100C>T MANE Select	ENSP00000495195.1:p.Ser1700=
ENST00000373965.6:c.4911C>T	ENSP00000363076.3:p.Ser1637=
ENST00000414778.5:c.4908C>T	ENSP00000410304.2:p.Ser1636=
ENST00000495484.5:c.1128C>T	ENSP00000480780.1:p.Ser376=
ENST00000614895.4:c.4923C>T	ENSP00000478512.1:p.Ser1641=
ENST00000616114.4:c.4905C>T	ENSP00000483745.1:p.Ser1635=
ENST00000618301.4:c.1260C>T	ENSP00000482780.1:p.Ser420=
ENST00000621708.4:c.4926C>T	ENSP00000484454.1:p.Ser1642=
NM_001142771.1:c.4926C>T	NP_001136243.1:p.Ser1642=
NM_001142772.1:c.4911C>T	NP_001136244.1:p.Ser1637=
NM_001354420.1:c.4905C>T	NP_001341349.1:p.Ser1635=
NM_001354429.1:c.5034C>T	NP_001341358.1:p.Ser1678=
XR_001747192.2:n.11392C>T
XR_001747193.2:n.11383C>T
NM_001142771.2:c.4926C>T	NP_001136243.1:p.Ser1642=
NM_001142772.2:c.4911C>T	NP_001136244.1:p.Ser1637=
NM_001354420.2:c.4905C>T	NP_001341349.1:p.Ser1635=
NM_001354429.2:c.5034C>T	NP_001341358.1:p.Ser1678=
NM_001384140.1:c.5100C>T MANE Select	NP_001371069.1:p.Ser1700=