Canonical Allele Identifier: CA2470555342
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735676G= , CM000686.2:g.12735676G= GRCh38
NC_000024.9:g.14847610G= , CM000686.1:g.14847610G= GRCh37
NC_000024.8:g.13357004G= NCBI36
NG_008311.1:g.39451G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.722G= ENSP00000498372.1:p.Arg241=
ENST00000338981.7:c.722G= MANE Select ENSP00000342812.3:p.Arg241=
ENST00000426564.6:n.734G=
NM_004654.3:c.722G= NP_004645.2:p.Arg241=
XM_011531469.1:c.722G= XP_011529771.1:p.Arg241=
XM_011531470.1:c.488G= XP_011529772.1:p.Arg163=
XM_017030078.2:c.722G= XP_016885567.1:p.Arg241=
NM_004654.4:c.722G= MANE Select NP_004645.2:p.Arg241=