Canonical Allele Identifier: CA2444796969

Gene: PCDH11X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.91809193A= , CM000685.2:g.91809193A=	GRCh38
NC_000023.10:g.91064192A= , CM000685.1:g.91064192A=	GRCh37
NC_000023.9:g.90950848A=	NCBI36
NG_016251.1:g.34933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682573.1:c.-378-273A= MANE Select	ENSP00000507225.1:n.-378-273A=
ENST00000298274.12:n.425-1280A=
ENST00000395337.6:c.-209-1280A=	ENSP00000378746.4:n.-209-1280A=
XM_011530910.1:c.-122-1280A=	XP_011529212.1:n.-122-1280A=
XM_011530911.1:c.-291-273A=	XP_011529213.1:n.-291-273A=
XM_011530912.1:c.-291-273A=	XP_011529214.1:n.-291-273A=
XM_011530913.1:c.-291-273A=	XP_011529215.1:n.-291-273A=
XM_011530914.1:c.-44-26268A=	XP_011529216.1:n.-44-26268A=
XM_011530915.1:c.-291-273A=	XP_011529217.1:n.-291-273A=
XM_011530916.1:c.-122-1280A=	XP_011529218.1:n.-122-1280A=
XM_011530911.2:c.-291-273A=	XP_011529213.1:n.-291-273A=
XM_011530912.2:c.-291-273A=	XP_011529214.1:n.-291-273A=
XM_011530913.2:c.-291-273A=	XP_011529215.1:n.-291-273A=
XM_011530914.2:c.-44-26268A=	XP_011529216.1:n.-44-26268A=
XM_011530915.2:c.-291-273A=	XP_011529217.1:n.-291-273A=
XM_011530916.2:c.-122-1280A=	XP_011529218.1:n.-122-1280A=
XM_017029417.1:c.-291-273A=	XP_016884906.1:n.-291-273A=
XM_017029418.1:c.-291-273A=	XP_016884907.1:n.-291-273A=
XM_017029420.1:c.-291-273A=	XP_016884909.1:n.-291-273A=
XM_017029422.1:c.-44-26268A=	XP_016884911.1:n.-44-26268A=
NM_032968.5:c.-378-273A= MANE Select	NP_116750.1:n.-378-273A=