Canonical Allele Identifier: CA2469802161

Gene: PCDH11Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.5101434T= , CM000686.2:g.5101434T=	GRCh38
NC_000024.9:g.4969475T= , CM000686.1:g.4969475T=	GRCh37
NC_000024.8:g.5029475T=	NCBI36
NG_011652.1:g.106209T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698851.1:c.2853+727T= MANE Select	ENSP00000513983.1:n.2853+727T=
ENST00000215473.7:c.*694T=	ENSP00000215473.7:n.*694T=
ENST00000333703.8:c.3096+727T=	ENSP00000330552.4:n.3096+727T=
ENST00000362095.9:c.3129+727T=	ENSP00000355419.5:n.3129+727T=
ENST00000400457.3:c.3129+727T=	ENSP00000383306.3:n.3129+727T=
ENST00000622698.4:c.3096+727T=	ENSP00000482115.1:n.3096+727T=
NM_001278619.1:c.3096+727T=	NP_001265548.1:n.3096+727T=
NM_032971.2:c.3096+727T=	NP_116753.1:n.3096+727T=
NM_032972.2:c.3129+727T=	NP_116754.1:n.3129+727T=
NM_032973.2:c.3129+727T=	NP_116755.1:n.3129+727T=
XM_011531476.1:c.3096+727T=	XP_011529778.1:n.3096+727T=
XM_011531477.1:c.3096+727T=	XP_011529779.1:n.3096+727T=
XM_011531478.1:c.2853+727T=	XP_011529780.1:n.2853+727T=
XM_017030079.1:c.3096+727T=	XP_016885568.1:n.3096+727T=
XM_017030080.1:c.3096+727T=	XP_016885569.1:n.3096+727T=
XM_017030081.1:c.3096+727T=	XP_016885570.1:n.3096+727T=
XM_017030082.1:c.3096+727T=	XP_016885571.1:n.3096+727T=
XM_017030083.1:c.2853+727T=	XP_016885572.1:n.2853+727T=
NM_001278619.2:c.3096+727T=	NP_001265548.1:n.3096+727T=
NM_032971.3:c.3096+727T=	NP_116753.1:n.3096+727T=
NM_032972.3:c.3129+727T=	NP_116754.1:n.3129+727T=
NM_001395587.1:c.2853+727T= MANE Select	NP_001382516.1:n.2853+727T=