Canonical Allele Identifier: CA337501708
Gene: PCDH11Y HGNC NCBI

Linked Data

dbSNP Id: rs182668234
gnomAD v3: Y-5034265-A-C
gnomAD v4: Y-5034265-A-C
MyVariant Identifiers: chrY:g.4902306A>C (hg19) chrY:g.5034265A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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