Canonical Allele Identifier: CA414980522
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14832541C>A (hg19) chrY:g.12720608C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720608C>A , CM000686.2:g.12720608C>A GRCh38
NC_000024.9:g.14832541C>A , CM000686.1:g.14832541C>A GRCh37
NC_000024.8:g.13341935C>A NCBI36
NG_008311.1:g.24382C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.116C>A ENSP00000498372.1:p.Ser39Tyr
ENST00000338981.7:c.116C>A MANE Select ENSP00000342812.3:p.Ser39Tyr
ENST00000426564.6:n.128C>A
ENST00000493168.1:n.192C>A
NM_004654.3:c.116C>A NP_004645.2:p.Ser39Tyr
XM_011531469.1:c.116C>A XP_011529771.1:p.Ser39Tyr
XM_011531470.1:c.-119C>A XP_011529772.1:n.-119C>A
XM_017030078.2:c.116C>A XP_016885567.1:p.Ser39Tyr
NM_004654.4:c.116C>A MANE Select NP_004645.2:p.Ser39Tyr
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