Canonical Allele Identifier: CA469545235

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566363G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806603G>T , CM000672.2:g.53806603G>T	GRCh38
NC_000010.10:g.55566363G>T , CM000672.1:g.55566363G>T	GRCh37
NC_000010.9:g.55236369G>T	NCBI36
NG_009191.2:g.999689C>A
NG_009191.3:g.1827580C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.4058C>A
ENST00000644397.2:c.5199C>A MANE Select	ENSP00000495195.1:p.Leu1733=
ENST00000373965.6:c.5010C>A	ENSP00000363076.3:p.Leu1670=
ENST00000414778.5:c.5007C>A	ENSP00000410304.2:p.Leu1669=
ENST00000495484.5:c.1227C>A	ENSP00000480780.1:p.Leu409=
ENST00000614895.4:c.5022C>A	ENSP00000478512.1:p.Leu1674=
ENST00000616114.4:c.5004C>A	ENSP00000483745.1:p.Leu1668=
ENST00000618301.4:c.1359C>A	ENSP00000482780.1:p.Leu453=
ENST00000621708.4:c.5025C>A	ENSP00000484454.1:p.Leu1675=
NM_001142771.1:c.5025C>A	NP_001136243.1:p.Leu1675=
NM_001142772.1:c.5010C>A	NP_001136244.1:p.Leu1670=
NM_001354420.1:c.5004C>A	NP_001341349.1:p.Leu1668=
NM_001354429.1:c.5133C>A	NP_001341358.1:p.Leu1711=
XR_001747192.2:n.11491C>A
XR_001747193.2:n.11482C>A
NM_001142771.2:c.5025C>A	NP_001136243.1:p.Leu1675=
NM_001142772.2:c.5010C>A	NP_001136244.1:p.Leu1670=
NM_001354420.2:c.5004C>A	NP_001341349.1:p.Leu1668=
NM_001354429.2:c.5133C>A	NP_001341358.1:p.Leu1711=
NM_001384140.1:c.5199C>A MANE Select	NP_001371069.1:p.Leu1733=