Canonical Allele Identifier: CA2444918323

Gene: PCDH11X

Linked Data

• dbSNP Id: rs2065124538

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.92138692_92138696del , CM000685.2:g.92138692_92138696del	GRCh38
NC_000023.10:g.91393691_91393695del , CM000685.1:g.91393691_91393695del	GRCh37
NC_000023.9:g.91280347_91280351del	NCBI36
NG_016251.1:g.364432_364436del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682573.1:c.3034-62683_3034-62679del MANE Select	ENSP00000507225.1:n.3034-62683_3034-62679...
ENST00000361655.6:c.3034-62683_3034-62679del	ENSP00000355105.2:n.3034-62683_3034-62679...
ENST00000373088.5:c.3034-249043_3034-249039del	ENSP00000362180.1:n.3034-249043_3034-2490...
ENST00000373094.5:c.3034-62683_3034-62679del	ENSP00000362186.1:n.3034-62683_3034-62679...
ENST00000373097.5:c.3034-62683_3034-62679del	ENSP00000362189.1:n.3034-62683_3034-62679...
ENST00000406881.3:c.3034-62683_3034-62679del	ENSP00000384758.1:n.3034-62683_3034-62679...
ENST00000504220.6:c.3034-62683_3034-62679del	ENSP00000423762.1:n.3034-62683_3034-62679...
NM_001168360.1:c.3034-62683_3034-62679del	NP_001161832.1:n.3034-62683_3034-62679del...
NM_001168361.1:c.3034-62683_3034-62679del	NP_001161833.1:n.3034-62683_3034-62679del...
NM_001168362.1:c.3034-249043_3034-249039del	NP_001161834.1:n.3034-249043_3034-249039d...
NM_001168363.1:c.3034-62683_3034-62679del	NP_001161835.1:n.3034-62683_3034-62679del...
NM_032968.4:c.3034-62683_3034-62679del	NP_116750.1:n.3034-62683_3034-62679del
NM_032969.4:c.3034-62683_3034-62679del	NP_116751.1:n.3034-62683_3034-62679del
XM_011530910.1:c.3121-62683_3121-62679del	XP_011529212.1:n.3121-62683_3121-62679del...
XM_011530911.1:c.3121-62683_3121-62679del	XP_011529213.1:n.3121-62683_3121-62679del...
XM_011530912.1:c.3121-62683_3121-62679del	XP_011529214.1:n.3121-62683_3121-62679del...
XM_011530913.1:c.3121-62683_3121-62679del	XP_011529215.1:n.3121-62683_3121-62679del...
XM_011530914.1:c.3034-62683_3034-62679del	XP_011529216.1:n.3034-62683_3034-62679del...
XM_011530911.2:c.3121-62683_3121-62679del	XP_011529213.1:n.3121-62683_3121-62679del...
XM_011530912.2:c.3121-62683_3121-62679del	XP_011529214.1:n.3121-62683_3121-62679del...
XM_011530913.2:c.3121-62683_3121-62679del	XP_011529215.1:n.3121-62683_3121-62679del...
XM_011530914.2:c.3034-62683_3034-62679del	XP_011529216.1:n.3034-62683_3034-62679del...
XM_017029416.1:c.3034-62683_3034-62679del	XP_016884905.1:n.3034-62683_3034-62679del...
XM_017029417.1:c.3121-62683_3121-62679del	XP_016884906.1:n.3121-62683_3121-62679del...
XM_017029418.1:c.3121-62683_3121-62679del	XP_016884907.1:n.3121-62683_3121-62679del...
XM_017029419.1:c.3034-249043_3034-249039del	XP_016884908.1:n.3034-249043_3034-249039d...
XM_017029420.1:c.3121-249043_3121-249039del	XP_016884909.1:n.3121-249043_3121-249039d...
XM_017029421.1:c.3034-62683_3034-62679del	XP_016884910.1:n.3034-62683_3034-62679del...
NM_032968.5:c.3034-62683_3034-62679del MANE Select	NP_116750.1:n.3034-62683_3034-62679del