Canonical Allele Identifier: CA376515976

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566446T>C (hg19) ; chr10:g.53806686T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806686T>C , CM000672.2:g.53806686T>C	GRCh38
NC_000010.10:g.55566446T>C , CM000672.1:g.55566446T>C	GRCh37
NC_000010.9:g.55236452T>C	NCBI36
NG_009191.2:g.999606A>G
NG_009191.3:g.1827497A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3975A>G
ENST00000644397.2:c.5116A>G MANE Select	ENSP00000495195.1:p.Asn1706Asp
ENST00000373965.6:c.4927A>G	ENSP00000363076.3:p.Asn1643Asp
ENST00000414778.5:c.4924A>G	ENSP00000410304.2:p.Asn1642Asp
ENST00000495484.5:c.1144A>G	ENSP00000480780.1:p.Asn382Asp
ENST00000614895.4:c.4939A>G	ENSP00000478512.1:p.Asn1647Asp
ENST00000616114.4:c.4921A>G	ENSP00000483745.1:p.Asn1641Asp
ENST00000618301.4:c.1276A>G	ENSP00000482780.1:p.Asn426Asp
ENST00000621708.4:c.4942A>G	ENSP00000484454.1:p.Asn1648Asp
NM_001142771.1:c.4942A>G	NP_001136243.1:p.Asn1648Asp
NM_001142772.1:c.4927A>G	NP_001136244.1:p.Asn1643Asp
NM_001354420.1:c.4921A>G	NP_001341349.1:p.Asn1641Asp
NM_001354429.1:c.5050A>G	NP_001341358.1:p.Asn1684Asp
XR_001747192.2:n.11408A>G
XR_001747193.2:n.11399A>G
NM_001142771.2:c.4942A>G	NP_001136243.1:p.Asn1648Asp
NM_001142772.2:c.4927A>G	NP_001136244.1:p.Asn1643Asp
NM_001354420.2:c.4921A>G	NP_001341349.1:p.Asn1641Asp
NM_001354429.2:c.5050A>G	NP_001341358.1:p.Asn1684Asp
NM_001384140.1:c.5116A>G MANE Select	NP_001371069.1:p.Asn1706Asp