Canonical Allele Identifier: CA337503224
Gene: PCDH11Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.5101434T>A
GRCh37 chrY:g.4969475T>A
gnomAD v3:
Y:5101434 T / A
gnomAD v4:
chrY-5101434-T-A
Joint Max Group AF 0.00634665 (AFR)
Genomes Max Group AF 0.00648776 (AFR)
Exomes Max Group AF 0.00332958 (AFR)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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