Canonical Allele Identifier: CA207194904

Gene: PCDH15

Linked Data

• dbSNP Id: rs569905861
• gnomAD v2: 10-55565923-TCTTA-T
• gnomAD v3: 10-53806163-TCTTA-T
• gnomAD v4: 10-53806163-TCTTA-T
• MyVariant Identifiers: chr10:g.55565924_55565927del (hg19) ; chr10:g.53806164_53806167del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806167_53806170del , CM000672.2:g.53806167_53806170del	GRCh38
NC_000010.10:g.55565927_55565930del , CM000672.1:g.55565927_55565930del	GRCh37
NC_000010.9:g.55235933_55235936del	NCBI36
NG_009191.2:g.1000125_1000128del
NG_009191.3:g.1828016_1828019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*412_*415del MANE Select	ENSP00000495195.1:n.*412_*415del
ENST00000373965.6:c.*412_*415del	ENSP00000363076.3:n.*412_*415del
ENST00000414778.5:c.*412_*415del	ENSP00000410304.2:n.*412_*415del
ENST00000614895.4:c.*412_*415del	ENSP00000478512.1:n.*412_*415del
ENST00000616114.4:c.*412_*415del	ENSP00000483745.1:n.*412_*415del
NM_001142771.1:c.*412_*415del	NP_001136243.1:n.*412_*415del
NM_001142772.1:c.*412_*415del	NP_001136244.1:n.*412_*415del
NM_001354420.1:c.*412_*415del	NP_001341349.1:n.*412_*415del
NM_001354429.1:c.*412_*415del	NP_001341358.1:n.*412_*415del
XR_001747192.2:n.11927_11930del
XR_001747193.2:n.11918_11921del
NM_001142771.2:c.*412_*415del	NP_001136243.1:n.*412_*415del
NM_001142772.2:c.*412_*415del	NP_001136244.1:n.*412_*415del
NM_001354420.2:c.*412_*415del	NP_001341349.1:n.*412_*415del
NM_001354429.2:c.*412_*415del	NP_001341358.1:n.*412_*415del
NM_001384140.1:c.*412_*415del MANE Select	NP_001371069.1:n.*412_*415del