Canonical Allele Identifier: CA879680667
Gene: PCDH11X HGNC NCBI

Linked Data

dbSNP Id: rs1288008674

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.92138798_92138818del , CM000685.2:g.92138798_92138818del GRCh38
NC_000023.10:g.91393797_91393817del , CM000685.1:g.91393797_91393817del GRCh37
NC_000023.9:g.91280453_91280473del NCBI36
NG_016251.1:g.364538_364558del

Transcript Alleles

HGVS Amino-acid change
ENST00000682573.1:c.3034-62577_3034-62557del MANE Select ENSP00000507225.1:n.3034-62577_3034-62557...
ENST00000361655.6:c.3034-62577_3034-62557del ENSP00000355105.2:n.3034-62577_3034-62557...
ENST00000373088.5:c.3034-248937_3034-248917del ENSP00000362180.1:n.3034-248937_3034-2489...
ENST00000373094.5:c.3034-62577_3034-62557del ENSP00000362186.1:n.3034-62577_3034-62557...
ENST00000373097.5:c.3034-62577_3034-62557del ENSP00000362189.1:n.3034-62577_3034-62557...
ENST00000406881.3:c.3034-62577_3034-62557del ENSP00000384758.1:n.3034-62577_3034-62557...
ENST00000504220.6:c.3034-62577_3034-62557del ENSP00000423762.1:n.3034-62577_3034-62557...
NM_001168360.1:c.3034-62577_3034-62557del NP_001161832.1:n.3034-62577_3034-62557del...
NM_001168361.1:c.3034-62577_3034-62557del NP_001161833.1:n.3034-62577_3034-62557del...
NM_001168362.1:c.3034-248937_3034-248917del NP_001161834.1:n.3034-248937_3034-248917d...
NM_001168363.1:c.3034-62577_3034-62557del NP_001161835.1:n.3034-62577_3034-62557del...
NM_032968.4:c.3034-62577_3034-62557del NP_116750.1:n.3034-62577_3034-62557del
NM_032969.4:c.3034-62577_3034-62557del NP_116751.1:n.3034-62577_3034-62557del
XM_011530910.1:c.3121-62577_3121-62557del XP_011529212.1:n.3121-62577_3121-62557del...
XM_011530911.1:c.3121-62577_3121-62557del XP_011529213.1:n.3121-62577_3121-62557del...
XM_011530912.1:c.3121-62577_3121-62557del XP_011529214.1:n.3121-62577_3121-62557del...
XM_011530913.1:c.3121-62577_3121-62557del XP_011529215.1:n.3121-62577_3121-62557del...
XM_011530914.1:c.3034-62577_3034-62557del XP_011529216.1:n.3034-62577_3034-62557del...
XM_011530911.2:c.3121-62577_3121-62557del XP_011529213.1:n.3121-62577_3121-62557del...
XM_011530912.2:c.3121-62577_3121-62557del XP_011529214.1:n.3121-62577_3121-62557del...
XM_011530913.2:c.3121-62577_3121-62557del XP_011529215.1:n.3121-62577_3121-62557del...
XM_011530914.2:c.3034-62577_3034-62557del XP_011529216.1:n.3034-62577_3034-62557del...
XM_017029416.1:c.3034-62577_3034-62557del XP_016884905.1:n.3034-62577_3034-62557del...
XM_017029417.1:c.3121-62577_3121-62557del XP_016884906.1:n.3121-62577_3121-62557del...
XM_017029418.1:c.3121-62577_3121-62557del XP_016884907.1:n.3121-62577_3121-62557del...
XM_017029419.1:c.3034-248937_3034-248917del XP_016884908.1:n.3034-248937_3034-248917d...
XM_017029420.1:c.3121-248937_3121-248917del XP_016884909.1:n.3121-248937_3121-248917d...
XM_017029421.1:c.3034-62577_3034-62557del XP_016884910.1:n.3034-62577_3034-62557del...
NM_032968.5:c.3034-62577_3034-62557del MANE Select NP_116750.1:n.3034-62577_3034-62557del