Canonical Allele Identifier: CA469545862

Gene: PCDH15

Linked Data

• dbSNP Id: rs1841189089
• MyVariant Identifiers: chr10:g.55566477T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806717T>C , CM000672.2:g.53806717T>C	GRCh38
NC_000010.10:g.55566477T>C , CM000672.1:g.55566477T>C	GRCh37
NC_000010.9:g.55236483T>C	NCBI36
NG_009191.2:g.999575A>G
NG_009191.3:g.1827466A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3944A>G
ENST00000644397.2:c.5085A>G MANE Select	ENSP00000495195.1:p.Thr1695=
ENST00000373965.6:c.4896A>G	ENSP00000363076.3:p.Thr1632=
ENST00000414778.5:c.4893A>G	ENSP00000410304.2:p.Thr1631=
ENST00000495484.5:c.1113A>G	ENSP00000480780.1:p.Thr371=
ENST00000614895.4:c.4908A>G	ENSP00000478512.1:p.Thr1636=
ENST00000616114.4:c.4890A>G	ENSP00000483745.1:p.Thr1630=
ENST00000618301.4:c.1245A>G	ENSP00000482780.1:p.Thr415=
ENST00000621708.4:c.4911A>G	ENSP00000484454.1:p.Thr1637=
NM_001142771.1:c.4911A>G	NP_001136243.1:p.Thr1637=
NM_001142772.1:c.4896A>G	NP_001136244.1:p.Thr1632=
NM_001354420.1:c.4890A>G	NP_001341349.1:p.Thr1630=
NM_001354429.1:c.5019A>G	NP_001341358.1:p.Thr1673=
XR_001747192.2:n.11377A>G
XR_001747193.2:n.11368A>G
NM_001142771.2:c.4911A>G	NP_001136243.1:p.Thr1637=
NM_001142772.2:c.4896A>G	NP_001136244.1:p.Thr1632=
NM_001354420.2:c.4890A>G	NP_001341349.1:p.Thr1630=
NM_001354429.2:c.5019A>G	NP_001341358.1:p.Thr1673=
NM_001384140.1:c.5085A>G MANE Select	NP_001371069.1:p.Thr1695=