Canonical Allele Identifier: CA1910754773
Gene: PCDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1841142774

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806202_53806205dup , CM000672.2:g.53806202_53806205dup GRCh38
NC_000010.10:g.55565962_55565965dup , CM000672.1:g.55565962_55565965dup GRCh37
NC_000010.9:g.55235968_55235971dup NCBI36
NG_009191.2:g.1000088_1000091dup
NG_009191.3:g.1827979_1827982dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644397.2:c.*375_*378dup MANE Select ENSP00000495195.1:n.*375_*378dup
ENST00000373965.6:c.*375_*378dup ENSP00000363076.3:n.*375_*378dup
ENST00000414778.5:c.*375_*378dup ENSP00000410304.2:n.*375_*378dup
ENST00000614895.4:c.*375_*378dup ENSP00000478512.1:n.*375_*378dup
ENST00000616114.4:c.*375_*378dup ENSP00000483745.1:n.*375_*378dup
NM_001142771.1:c.*375_*378dup NP_001136243.1:n.*375_*378dup
NM_001142772.1:c.*375_*378dup NP_001136244.1:n.*375_*378dup
NM_001354420.1:c.*375_*378dup NP_001341349.1:n.*375_*378dup
NM_001354429.1:c.*375_*378dup NP_001341358.1:n.*375_*378dup
XR_001747192.2:n.11890_11893dup
XR_001747193.2:n.11881_11884dup
NM_001142771.2:c.*375_*378dup NP_001136243.1:n.*375_*378dup
NM_001142772.2:c.*375_*378dup NP_001136244.1:n.*375_*378dup
NM_001354420.2:c.*375_*378dup NP_001341349.1:n.*375_*378dup
NM_001354429.2:c.*375_*378dup NP_001341358.1:n.*375_*378dup
NM_001384140.1:c.*375_*378dup MANE Select NP_001371069.1:n.*375_*378dup