Canonical Allele Identifier: CA2470554563
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720608C= , CM000686.2:g.12720608C= GRCh38
NC_000024.9:g.14832541C= , CM000686.1:g.14832541C= GRCh37
NC_000024.8:g.13341935C= NCBI36
NG_008311.1:g.24382C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.116C= ENSP00000498372.1:p.Ser39=
ENST00000338981.7:c.116C= MANE Select ENSP00000342812.3:p.Ser39=
ENST00000426564.6:n.128C=
ENST00000493168.1:n.192C=
NM_004654.3:c.116C= NP_004645.2:p.Ser39=
XM_011531469.1:c.116C= XP_011529771.1:p.Ser39=
XM_011531470.1:c.-119C= XP_011529772.1:n.-119C=
XM_017030078.2:c.116C= XP_016885567.1:p.Ser39=
NM_004654.4:c.116C= MANE Select NP_004645.2:p.Ser39=