Canonical Allele Identifier: CA643234029

Gene: PCDH11X

Linked Data

• dbSNP Id: rs2524861
• gnomAD v2: X-91064190-C-A
• gnomAD v3: X-91809191-C-A
• gnomAD v4: X-91809191-C-A
• MyVariant Identifiers: chrX:g.91064190C>A (hg19) ; chrX:g.91809191C>A (hg38)

Genomic Alleles

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

Transcript Alleles

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