Canonical Allele Identifier: CA415007642
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778056T>A , CM000686.2:g.12778056T>A GRCh38
NC_000024.9:g.14889990T>A , CM000686.1:g.14889990T>A GRCh37
NC_000024.8:g.13399384T>A NCBI36
NG_008311.1:g.81831T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2677T>A ENSP00000498372.1:p.Phe893Ile
ENST00000338981.7:c.2677T>A MANE Select ENSP00000342812.3:p.Phe893Ile
ENST00000426564.6:n.2689T>A
NM_004654.3:c.2677T>A NP_004645.2:p.Phe893Ile
XM_011531469.1:c.2677T>A XP_011529771.1:p.Phe893Ile
XM_011531470.1:c.2443T>A XP_011529772.1:p.Phe815Ile
XM_017030078.2:c.2692T>A XP_016885567.1:p.Phe898Ile
NM_004654.4:c.2677T>A MANE Select NP_004645.2:p.Phe893Ile