Canonical Allele Identifier: CA2470555345
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735710A= , CM000686.2:g.12735710A= GRCh38
NC_000024.9:g.14847644A= , CM000686.1:g.14847644A= GRCh37
NC_000024.8:g.13357038A= NCBI36
NG_008311.1:g.39485A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.756A= ENSP00000498372.1:p.Ile252=
ENST00000338981.7:c.756A= MANE Select ENSP00000342812.3:p.Ile252=
ENST00000426564.6:n.768A=
NM_004654.3:c.756A= NP_004645.2:p.Ile252=
XM_011531469.1:c.756A= XP_011529771.1:p.Ile252=
XM_011531470.1:c.519+3A= XP_011529772.1:n.519+3A=
XM_017030078.2:c.756A= XP_016885567.1:p.Ile252=
NM_004654.4:c.756A= MANE Select NP_004645.2:p.Ile252=