Canonical Allele Identifier: CA2470554578
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720696T= , CM000686.2:g.12720696T= GRCh38
NC_000024.9:g.14832629T= , CM000686.1:g.14832629T= GRCh37
NC_000024.8:g.13342023T= NCBI36
NG_008311.1:g.24470T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.204T= ENSP00000498372.1:p.Phe68=
ENST00000338981.7:c.204T= MANE Select ENSP00000342812.3:p.Phe68=
ENST00000426564.6:n.216T=
ENST00000493168.1:n.280T=
NM_004654.3:c.204T= NP_004645.2:p.Phe68=
XM_011531469.1:c.204T= XP_011529771.1:p.Phe68=
XM_011531470.1:c.-31T= XP_011529772.1:n.-31T=
XM_017030078.2:c.204T= XP_016885567.1:p.Phe68=
NM_004654.4:c.204T= MANE Select NP_004645.2:p.Phe68=