Canonical Allele Identifier: CA469545869

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566488G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806728G>A , CM000672.2:g.53806728G>A	GRCh38
NC_000010.10:g.55566488G>A , CM000672.1:g.55566488G>A	GRCh37
NC_000010.9:g.55236494G>A	NCBI36
NG_009191.2:g.999564C>T
NG_009191.3:g.1827455C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3933C>T
ENST00000644397.2:c.5074C>T MANE Select	ENSP00000495195.1:p.Leu1692=
ENST00000373965.6:c.4885C>T	ENSP00000363076.3:p.Leu1629=
ENST00000414778.5:c.4882C>T	ENSP00000410304.2:p.Leu1628=
ENST00000495484.5:c.1102C>T	ENSP00000480780.1:p.Leu368=
ENST00000614895.4:c.4897C>T	ENSP00000478512.1:p.Leu1633=
ENST00000616114.4:c.4879C>T	ENSP00000483745.1:p.Leu1627=
ENST00000618301.4:c.1234C>T	ENSP00000482780.1:p.Leu412=
ENST00000621708.4:c.4900C>T	ENSP00000484454.1:p.Leu1634=
NM_001142771.1:c.4900C>T	NP_001136243.1:p.Leu1634=
NM_001142772.1:c.4885C>T	NP_001136244.1:p.Leu1629=
NM_001354420.1:c.4879C>T	NP_001341349.1:p.Leu1627=
NM_001354429.1:c.5008C>T	NP_001341358.1:p.Leu1670=
XR_001747192.2:n.11366C>T
XR_001747193.2:n.11357C>T
NM_001142771.2:c.4900C>T	NP_001136243.1:p.Leu1634=
NM_001142772.2:c.4885C>T	NP_001136244.1:p.Leu1629=
NM_001354420.2:c.4879C>T	NP_001341349.1:p.Leu1627=
NM_001354429.2:c.5008C>T	NP_001341358.1:p.Leu1670=
NM_001384140.1:c.5074C>T MANE Select	NP_001371069.1:p.Leu1692=