Canonical Allele Identifier: CA376515733

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566369G>T (hg19) ; chr10:g.53806609G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806609G>T , CM000672.2:g.53806609G>T	GRCh38
NC_000010.10:g.55566369G>T , CM000672.1:g.55566369G>T	GRCh37
NC_000010.9:g.55236375G>T	NCBI36
NG_009191.2:g.999683C>A
NG_009191.3:g.1827574C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.4052C>A
ENST00000644397.2:c.5193C>A MANE Select	ENSP00000495195.1:p.Asn1731Lys
ENST00000373965.6:c.5004C>A	ENSP00000363076.3:p.Asn1668Lys
ENST00000414778.5:c.5001C>A	ENSP00000410304.2:p.Asn1667Lys
ENST00000495484.5:c.1221C>A	ENSP00000480780.1:p.Asn407Lys
ENST00000614895.4:c.5016C>A	ENSP00000478512.1:p.Asn1672Lys
ENST00000616114.4:c.4998C>A	ENSP00000483745.1:p.Asn1666Lys
ENST00000618301.4:c.1353C>A	ENSP00000482780.1:p.Asn451Lys
ENST00000621708.4:c.5019C>A	ENSP00000484454.1:p.Asn1673Lys
NM_001142771.1:c.5019C>A	NP_001136243.1:p.Asn1673Lys
NM_001142772.1:c.5004C>A	NP_001136244.1:p.Asn1668Lys
NM_001354420.1:c.4998C>A	NP_001341349.1:p.Asn1666Lys
NM_001354429.1:c.5127C>A	NP_001341358.1:p.Asn1709Lys
XR_001747192.2:n.11485C>A
XR_001747193.2:n.11476C>A
NM_001142771.2:c.5019C>A	NP_001136243.1:p.Asn1673Lys
NM_001142772.2:c.5004C>A	NP_001136244.1:p.Asn1668Lys
NM_001354420.2:c.4998C>A	NP_001341349.1:p.Asn1666Lys
NM_001354429.2:c.5127C>A	NP_001341358.1:p.Asn1709Lys
NM_001384140.1:c.5193C>A MANE Select	NP_001371069.1:p.Asn1731Lys