Canonical Allele Identifier: CA2579747614
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735609_12735610del , CM000686.2:g.12735609_12735610del GRCh38
NC_000024.9:g.14847543_14847544del , CM000686.1:g.14847543_14847544del GRCh37
NC_000024.8:g.13356937_13356938del NCBI36
NG_008311.1:g.39384_39385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.658-3_658-2del ENSP00000498372.1:n.658-3_658-2del
ENST00000338981.7:c.658-3_658-2del MANE Select ENSP00000342812.3:n.658-3_658-2del
ENST00000426564.6:n.670-3_670-2del
NM_004654.3:c.658-3_658-2del NP_004645.2:n.658-3_658-2del
XM_011531469.1:c.658-3_658-2del XP_011529771.1:n.658-3_658-2del
XM_011531470.1:c.424-3_424-2del XP_011529772.1:n.424-3_424-2del
XM_017030078.2:c.658-3_658-2del XP_016885567.1:n.658-3_658-2del
NM_004654.4:c.658-3_658-2del MANE Select NP_004645.2:n.658-3_658-2del