Canonical Allele Identifier: CA2766240778
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735860T>A , CM000686.2:g.12735860T>A GRCh38
NC_000024.9:g.14847794T>A , CM000686.1:g.14847794T>A GRCh37
NC_000024.8:g.13357188T>A NCBI36
NG_008311.1:g.39635T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.773+133T>A ENSP00000498372.1:n.773+133T>A
ENST00000338981.7:c.773+133T>A MANE Select ENSP00000342812.3:n.773+133T>A
ENST00000426564.6:n.785+133T>A
NM_004654.3:c.773+133T>A NP_004645.2:n.773+133T>A
XM_011531469.1:c.773+133T>A XP_011529771.1:n.773+133T>A
XM_011531470.1:c.539+67T>A XP_011529772.1:n.539+67T>A
XM_017030078.2:c.773+133T>A XP_016885567.1:n.773+133T>A
NM_004654.4:c.773+133T>A MANE Select NP_004645.2:n.773+133T>A
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