Canonical Allele Identifier: CA469545916

Gene: PCDH15

Linked Data

• gnomAD v4: 10-53806795-A-C
• MyVariant Identifiers: chr10:g.55566555A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806795A>C , CM000672.2:g.53806795A>C	GRCh38
NC_000010.10:g.55566555A>C , CM000672.1:g.55566555A>C	GRCh37
NC_000010.9:g.55236561A>C	NCBI36
NG_009191.2:g.999497T>G
NG_009191.3:g.1827388T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3866T>G
ENST00000644397.2:c.5007T>G MANE Select	ENSP00000495195.1:p.Thr1669=
ENST00000373965.6:c.4818T>G	ENSP00000363076.3:p.Thr1606=
ENST00000414778.5:c.4815T>G	ENSP00000410304.2:p.Thr1605=
ENST00000495484.5:c.1035T>G	ENSP00000480780.1:p.Thr345=
ENST00000614895.4:c.4830T>G	ENSP00000478512.1:p.Thr1610=
ENST00000616114.4:c.4812T>G	ENSP00000483745.1:p.Thr1604=
ENST00000618301.4:c.1167T>G	ENSP00000482780.1:p.Thr389=
ENST00000621708.4:c.4833T>G	ENSP00000484454.1:p.Thr1611=
NM_001142771.1:c.4833T>G	NP_001136243.1:p.Thr1611=
NM_001142772.1:c.4818T>G	NP_001136244.1:p.Thr1606=
NM_001354420.1:c.4812T>G	NP_001341349.1:p.Thr1604=
NM_001354429.1:c.4941T>G	NP_001341358.1:p.Thr1647=
XR_001747192.2:n.11299T>G
XR_001747193.2:n.11290T>G
NM_001142771.2:c.4833T>G	NP_001136243.1:p.Thr1611=
NM_001142772.2:c.4818T>G	NP_001136244.1:p.Thr1606=
NM_001354420.2:c.4812T>G	NP_001341349.1:p.Thr1604=
NM_001354429.2:c.4941T>G	NP_001341358.1:p.Thr1647=
NM_001384140.1:c.5007T>G MANE Select	NP_001371069.1:p.Thr1669=