Canonical Allele Identifier: CA2609218154

Gene: PCDH15

Linked Data

• gnomAD v4: 10-53806324-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806324C>T , CM000672.2:g.53806324C>T	GRCh38
NC_000010.10:g.55566084C>T , CM000672.1:g.55566084C>T	GRCh37
NC_000010.9:g.55236090C>T	NCBI36
NG_009191.2:g.999968G>A
NG_009191.3:g.1827859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*255G>A MANE Select	ENSP00000495195.1:n.*255G>A
ENST00000373965.6:c.*255G>A	ENSP00000363076.3:n.*255G>A
ENST00000414778.5:c.*255G>A	ENSP00000410304.2:n.*255G>A
ENST00000614895.4:c.*255G>A	ENSP00000478512.1:n.*255G>A
ENST00000616114.4:c.*255G>A	ENSP00000483745.1:n.*255G>A
ENST00000621708.4:c.*255G>A	ENSP00000484454.1:n.*255G>A
NM_001142771.1:c.*255G>A	NP_001136243.1:n.*255G>A
NM_001142772.1:c.*255G>A	NP_001136244.1:n.*255G>A
NM_001354420.1:c.*255G>A	NP_001341349.1:n.*255G>A
NM_001354429.1:c.*255G>A	NP_001341358.1:n.*255G>A
XR_001747192.2:n.11770G>A
XR_001747193.2:n.11761G>A
NM_001142771.2:c.*255G>A	NP_001136243.1:n.*255G>A
NM_001142772.2:c.*255G>A	NP_001136244.1:n.*255G>A
NM_001354420.2:c.*255G>A	NP_001341349.1:n.*255G>A
NM_001354429.2:c.*255G>A	NP_001341358.1:n.*255G>A
NM_001384140.1:c.*255G>A MANE Select	NP_001371069.1:n.*255G>A