Canonical Allele Identifier: CA332638854

Gene: PCDH11X

Linked Data

• dbSNP Id: rs2524861
• MyVariant Identifiers: chrX:g.91064190C>G (hg19) ; chrX:g.91809191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.91809191C>G , CM000685.2:g.91809191C>G	GRCh38
NC_000023.10:g.91064190C>G , CM000685.1:g.91064190C>G	GRCh37
NC_000023.9:g.90950846C>G	NCBI36
NG_016251.1:g.34931C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682573.1:c.-378-275C>G MANE Select	ENSP00000507225.1:n.-378-275C>G
ENST00000298274.12:n.425-1282C>G
ENST00000395337.6:c.-209-1282C>G	ENSP00000378746.4:n.-209-1282C>G
XM_011530910.1:c.-122-1282C>G	XP_011529212.1:n.-122-1282C>G
XM_011530911.1:c.-291-275C>G	XP_011529213.1:n.-291-275C>G
XM_011530912.1:c.-291-275C>G	XP_011529214.1:n.-291-275C>G
XM_011530913.1:c.-291-275C>G	XP_011529215.1:n.-291-275C>G
XM_011530914.1:c.-44-26270C>G	XP_011529216.1:n.-44-26270C>G
XM_011530915.1:c.-291-275C>G	XP_011529217.1:n.-291-275C>G
XM_011530916.1:c.-122-1282C>G	XP_011529218.1:n.-122-1282C>G
XM_011530911.2:c.-291-275C>G	XP_011529213.1:n.-291-275C>G
XM_011530912.2:c.-291-275C>G	XP_011529214.1:n.-291-275C>G
XM_011530913.2:c.-291-275C>G	XP_011529215.1:n.-291-275C>G
XM_011530914.2:c.-44-26270C>G	XP_011529216.1:n.-44-26270C>G
XM_011530915.2:c.-291-275C>G	XP_011529217.1:n.-291-275C>G
XM_011530916.2:c.-122-1282C>G	XP_011529218.1:n.-122-1282C>G
XM_017029417.1:c.-291-275C>G	XP_016884906.1:n.-291-275C>G
XM_017029418.1:c.-291-275C>G	XP_016884907.1:n.-291-275C>G
XM_017029420.1:c.-291-275C>G	XP_016884909.1:n.-291-275C>G
XM_017029422.1:c.-44-26270C>G	XP_016884911.1:n.-44-26270C>G
NM_032968.5:c.-378-275C>G MANE Select	NP_116750.1:n.-378-275C>G