Canonical Allele Identifier: CA1911387109
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55089191G= , CM000672.2:g.55089191G= GRCh38
NC_000010.10:g.56848951G= , CM000672.1:g.56848951G= GRCh37
NC_000010.9:g.56518957G= NCBI36
NG_009191.3:g.544992C=

Transcript Alleles

HGVS Amino-acid change
ENST00000458638.1:c.-80+77385C= ENSP00000394465.1:n.-80+77385C=
ENST00000613346.4:c.-80+77385C= ENSP00000481211.1:n.-80+77385C=
NM_001354404.1:c.-80+77385C= NP_001341333.1:n.-80+77385C=
XM_017016573.2:c.-157+77385C= XP_016872062.1:n.-157+77385C=
NM_001354404.2:c.-80+77385C= NP_001341333.1:n.-80+77385C=