Canonical Allele Identifier: CA415009085
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778210C>A , CM000686.2:g.12778210C>A GRCh38
NC_000024.9:g.14890144C>A , CM000686.1:g.14890144C>A GRCh37
NC_000024.8:g.13399538C>A NCBI36
NG_008311.1:g.81985C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2831C>A ENSP00000498372.1:p.Ser944Tyr
ENST00000338981.7:c.2831C>A MANE Select ENSP00000342812.3:p.Ser944Tyr
ENST00000426564.6:n.2843C>A
NM_004654.3:c.2831C>A NP_004645.2:p.Ser944Tyr
XM_011531469.1:c.2831C>A XP_011529771.1:p.Ser944Tyr
XM_011531470.1:c.2597C>A XP_011529772.1:p.Ser866Tyr
XM_017030078.2:c.2846C>A XP_016885567.1:p.Ser949Tyr
NM_004654.4:c.2831C>A MANE Select NP_004645.2:p.Ser944Tyr