Canonical Allele Identifier: CA2469827315

Gene: PCDH11Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.5499864A= , CM000686.2:g.5499864A=	GRCh38
NC_000024.9:g.5367905A= , CM000686.1:g.5367905A=	GRCh37
NC_000024.8:g.5427905A=	NCBI36
NG_011652.1:g.504639A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698851.1:c.2854-1193A= MANE Select	ENSP00000513983.1:n.2854-1193A=
ENST00000400457.3:c.3130-1193A=	ENSP00000383306.3:n.3130-1193A=
NM_032973.2:c.3130-1193A=	NP_116755.1:n.3130-1193A=
XM_011531476.1:c.3097-1193A=	XP_011529778.1:n.3097-1193A=
XM_011531477.1:c.3097-1193A=	XP_011529779.1:n.3097-1193A=
XM_011531478.1:c.2854-1193A=	XP_011529780.1:n.2854-1193A=
XM_017030079.1:c.3097-1193A=	XP_016885568.1:n.3097-1193A=
XM_017030080.1:c.3097-1193A=	XP_016885569.1:n.3097-1193A=
XM_017030081.1:c.3097-1193A=	XP_016885570.1:n.3097-1193A=
NM_001395587.1:c.2854-1193A= MANE Select	NP_001382516.1:n.2854-1193A=