Canonical Allele Identifier: CA337502814
Gene: PCDH11Y HGNC NCBI

Linked Data

dbSNP Id: rs2563344
gnomAD v3: Y-5089567-G-A
gnomAD v4: Y-5089567-G-A
MyVariant Identifiers: chrY:g.4957608G>A (hg19) chrY:g.5089567G>A (hg38)
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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
ENST00000698851.1:c.361-8648G>A MANE Select ENSP00000513983.1:n.361-8648G>A
ENST00000698927.1:c.604-8648G>A ENSP00000514038.1:n.604-8648G>A
ENST00000215473.7:c.637-8648G>A ENSP00000215473.7:n.637-8648G>A
ENST00000333703.8:c.604-8648G>A ENSP00000330552.4:n.604-8648G>A
ENST00000362095.9:c.637-8648G>A ENSP00000355419.5:n.637-8648G>A
ENST00000400457.3:c.637-8648G>A ENSP00000383306.3:n.637-8648G>A
ENST00000622698.4:c.604-8648G>A ENSP00000482115.1:n.604-8648G>A
NM_001278619.1:c.604-8648G>A NP_001265548.1:n.604-8648G>A
NM_032971.2:c.604-8648G>A NP_116753.1:n.604-8648G>A
NM_032972.2:c.637-8648G>A NP_116754.1:n.637-8648G>A
NM_032973.2:c.637-8648G>A NP_116755.1:n.637-8648G>A
XM_011531476.1:c.604-8648G>A XP_011529778.1:n.604-8648G>A
XM_011531477.1:c.604-8648G>A XP_011529779.1:n.604-8648G>A
XM_011531478.1:c.361-8648G>A XP_011529780.1:n.361-8648G>A
XM_017030079.1:c.604-8648G>A XP_016885568.1:n.604-8648G>A
XM_017030080.1:c.604-8648G>A XP_016885569.1:n.604-8648G>A
XM_017030081.1:c.604-8648G>A XP_016885570.1:n.604-8648G>A
XM_017030082.1:c.604-8648G>A XP_016885571.1:n.604-8648G>A
XM_017030083.1:c.361-8648G>A XP_016885572.1:n.361-8648G>A
NM_001278619.2:c.604-8648G>A NP_001265548.1:n.604-8648G>A
NM_032971.3:c.604-8648G>A NP_116753.1:n.604-8648G>A
NM_032972.3:c.637-8648G>A NP_116754.1:n.637-8648G>A
NM_001395587.1:c.361-8648G>A MANE Select NP_001382516.1:n.361-8648G>A
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