Canonical Allele Identifier: CA1910756027
Gene: PCDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806701T= , CM000672.2:g.53806701T= GRCh38
NC_000010.10:g.55566461T= , CM000672.1:g.55566461T= GRCh37
NC_000010.9:g.55236467T= NCBI36
NG_009191.2:g.999591A=
NG_009191.3:g.1827482A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642496.1:c.3960A=
ENST00000644397.2:c.5101A= MANE Select ENSP00000495195.1:p.Met1701=
ENST00000373965.6:c.4912A= ENSP00000363076.3:p.Met1638=
ENST00000414778.5:c.4909A= ENSP00000410304.2:p.Met1637=
ENST00000495484.5:c.1129A= ENSP00000480780.1:p.Met377=
ENST00000614895.4:c.4924A= ENSP00000478512.1:p.Met1642=
ENST00000616114.4:c.4906A= ENSP00000483745.1:p.Met1636=
ENST00000618301.4:c.1261A= ENSP00000482780.1:p.Met421=
ENST00000621708.4:c.4927A= ENSP00000484454.1:p.Met1643=
NM_001142771.1:c.4927A= NP_001136243.1:p.Met1643=
NM_001142772.1:c.4912A= NP_001136244.1:p.Met1638=
NM_001354420.1:c.4906A= NP_001341349.1:p.Met1636=
NM_001354429.1:c.5035A= NP_001341358.1:p.Met1679=
XR_001747192.2:n.11393A=
XR_001747193.2:n.11384A=
NM_001142771.2:c.4927A= NP_001136243.1:p.Met1643=
NM_001142772.2:c.4912A= NP_001136244.1:p.Met1638=
NM_001354420.2:c.4906A= NP_001341349.1:p.Met1636=
NM_001354429.2:c.5035A= NP_001341358.1:p.Met1679=
NM_001384140.1:c.5101A= MANE Select NP_001371069.1:p.Met1701=