Canonical Allele Identifier: CA414999279
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833857C>T , CM000686.2:g.12833857C>T GRCh38
NC_000024.9:g.14945783C>T , CM000686.1:g.14945783C>T GRCh37
NC_000024.8:g.13455177C>T NCBI36
NG_008311.1:g.137624C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5191C>T ENSP00000498372.1:p.His1731Tyr
ENST00000338981.7:c.5191C>T MANE Select ENSP00000342812.3:p.His1731Tyr
ENST00000426564.6:n.5203C>T
NM_004654.3:c.5191C>T NP_004645.2:p.His1731Tyr
XM_011531469.1:c.5191C>T XP_011529771.1:p.His1731Tyr
XM_011531470.1:c.4957C>T XP_011529772.1:p.His1653Tyr
XM_017030078.2:c.5206C>T XP_016885567.1:p.His1736Tyr
NM_004654.4:c.5191C>T MANE Select NP_004645.2:p.His1731Tyr