Canonical Allele Identifier: CA337502814
Gene: PCDH11Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2563344

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.5089567G>A , CM000686.2:g.5089567G>A GRCh38
NC_000024.9:g.4957608G>A , CM000686.1:g.4957608G>A GRCh37
NC_000024.8:g.5017608G>A NCBI36
NG_011652.1:g.94342G>A

Transcript Alleles

HGVS Amino-acid change
NM_001278619.1:c.604-8648G>A VV NP_001265548.1:p.=
NM_032971.2:c.604-8648G>A VV NP_116753.1:p.=
NM_032972.2:c.637-8648G>A VV NP_116754.1:p.=
NM_032973.2:c.637-8648G>A VV NP_116755.1:p.=
XM_011531476.1:c.604-8648G>A XP_011529778.1:p.=
XM_011531477.1:c.604-8648G>A XP_011529779.1:p.=
XM_011531478.1:c.361-8648G>A XP_011529780.1:p.=
XM_017030079.1:c.604-8648G>A XP_016885568.1:p.=
XM_017030080.1:c.604-8648G>A XP_016885569.1:p.=
XM_017030081.1:c.604-8648G>A XP_016885570.1:p.=
XM_017030082.1:c.604-8648G>A XP_016885571.1:p.=
XM_017030083.1:c.361-8648G>A XP_016885572.1:p.=
ENST00000215473.7:c.637-8648G>A ENSP00000215473.7:p.=
ENST00000333703.8:c.604-8648G>A ENSP00000330552.4:p.=
ENST00000362095.9:c.637-8648G>A ENSP00000355419.5:p.=
ENST00000400457.3:c.637-8648G>A ENSP00000383306.3:p.=
ENST00000622698.4:c.604-8648G>A ENSP00000482115.1:p.=