Canonical Allele Identifier: CA666450136

Gene: PCDH15

Linked Data

• dbSNP Id: rs1233578798
• gnomAD v4: 10-53806164-CTTACTTCTTT-C
• MyVariant Identifiers: chr10:g.55565925_55565934del (hg19) ; chr10:g.53806165_53806174del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806167_53806176del , CM000672.2:g.53806167_53806176del	GRCh38
NC_000010.10:g.55565927_55565936del , CM000672.1:g.55565927_55565936del	GRCh37
NC_000010.9:g.55235933_55235942del	NCBI36
NG_009191.2:g.1000118_1000127del
NG_009191.3:g.1828009_1828018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*405_*414del MANE Select	ENSP00000495195.1:n.*405_*414del
ENST00000373965.6:c.*405_*414del	ENSP00000363076.3:n.*405_*414del
ENST00000414778.5:c.*405_*414del	ENSP00000410304.2:n.*405_*414del
ENST00000614895.4:c.*405_*414del	ENSP00000478512.1:n.*405_*414del
ENST00000616114.4:c.*405_*414del	ENSP00000483745.1:n.*405_*414del
NM_001142771.1:c.*405_*414del	NP_001136243.1:n.*405_*414del
NM_001142772.1:c.*405_*414del	NP_001136244.1:n.*405_*414del
NM_001354420.1:c.*405_*414del	NP_001341349.1:n.*405_*414del
NM_001354429.1:c.*405_*414del	NP_001341358.1:n.*405_*414del
XR_001747192.2:n.11920_11929del
XR_001747193.2:n.11911_11920del
NM_001142771.2:c.*405_*414del	NP_001136243.1:n.*405_*414del
NM_001142772.2:c.*405_*414del	NP_001136244.1:n.*405_*414del
NM_001354420.2:c.*405_*414del	NP_001341349.1:n.*405_*414del
NM_001354429.2:c.*405_*414del	NP_001341358.1:n.*405_*414del
NM_001384140.1:c.*405_*414del MANE Select	NP_001371069.1:n.*405_*414del