Canonical Allele Identifier: CA414983469
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790422C>G , CM000686.2:g.12790422C>G GRCh38
NC_000024.9:g.14902355C>G , CM000686.1:g.14902355C>G GRCh37
NC_000024.8:g.13411749C>G NCBI36
NG_008311.1:g.94196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3577C>G ENSP00000498372.1:p.His1193Asp
ENST00000338981.7:c.3577C>G MANE Select ENSP00000342812.3:p.His1193Asp
ENST00000426564.6:n.3589C>G
NM_004654.3:c.3577C>G NP_004645.2:p.His1193Asp
XM_011531469.1:c.3577C>G XP_011529771.1:p.His1193Asp
XM_011531470.1:c.3343C>G XP_011529772.1:p.His1115Asp
XM_017030078.2:c.3592C>G XP_016885567.1:p.His1198Asp
NM_004654.4:c.3577C>G MANE Select NP_004645.2:p.His1193Asp