Canonical Allele Identifier: CA2469797382

Gene: PCDH11Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.5034265A= , CM000686.2:g.5034265A=	GRCh38
NC_000024.9:g.4902306A= , CM000686.1:g.4902306A=	GRCh37
NC_000024.8:g.4962306A=	NCBI36
NG_011652.1:g.39040A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698851.1:c.-211-22624A= MANE Select	ENSP00000513983.1:n.-211-22624A=
ENST00000698927.1:c.32+1537A=	ENSP00000514038.1:n.32+1537A=
ENST00000333703.8:c.32+1537A=	ENSP00000330552.4:n.32+1537A=
ENST00000621505.1:c.32+1537A=	ENSP00000478548.1:n.32+1537A=
ENST00000622698.4:c.32+1537A=	ENSP00000482115.1:n.32+1537A=
NM_001278619.1:c.32+1537A=	NP_001265548.1:n.32+1537A=
NM_032971.2:c.32+1537A=	NP_116753.1:n.32+1537A=
XM_011531476.1:c.32+1537A=	XP_011529778.1:n.32+1537A=
XM_011531477.1:c.32+1537A=	XP_011529779.1:n.32+1537A=
XM_011531478.1:c.-211-22624A=	XP_011529780.1:n.-211-22624A=
XM_017030079.1:c.32+1537A=	XP_016885568.1:n.32+1537A=
XM_017030080.1:c.32+1537A=	XP_016885569.1:n.32+1537A=
XM_017030081.1:c.32+1537A=	XP_016885570.1:n.32+1537A=
XM_017030082.1:c.32+1537A=	XP_016885571.1:n.32+1537A=
XM_017030083.1:c.-211-22624A=	XP_016885572.1:n.-211-22624A=
NM_001278619.2:c.32+1537A=	NP_001265548.1:n.32+1537A=
NM_032971.3:c.32+1537A=	NP_116753.1:n.32+1537A=
NM_001395587.1:c.-211-22624A= MANE Select	NP_001382516.1:n.-211-22624A=