Canonical Allele Identifier: CA415008371
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778135G>T , CM000686.2:g.12778135G>T GRCh38
NC_000024.9:g.14890069G>T , CM000686.1:g.14890069G>T GRCh37
NC_000024.8:g.13399463G>T NCBI36
NG_008311.1:g.81910G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2756G>T ENSP00000498372.1:p.Cys919Phe
ENST00000338981.7:c.2756G>T MANE Select ENSP00000342812.3:p.Cys919Phe
ENST00000426564.6:n.2768G>T
NM_004654.3:c.2756G>T NP_004645.2:p.Cys919Phe
XM_011531469.1:c.2756G>T XP_011529771.1:p.Cys919Phe
XM_011531470.1:c.2522G>T XP_011529772.1:p.Cys841Phe
XM_017030078.2:c.2771G>T XP_016885567.1:p.Cys924Phe
NM_004654.4:c.2756G>T MANE Select NP_004645.2:p.Cys919Phe