Canonical Allele Identifier: CA2579747616
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735722del , CM000686.2:g.12735722del GRCh38
NC_000024.9:g.14847656del , CM000686.1:g.14847656del GRCh37
NC_000024.8:g.13357050del NCBI36
NG_008311.1:g.39497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.768del ENSP00000498372.1:p.Ile257LeufsTer16
ENST00000338981.7:c.768del MANE Select ENSP00000342812.3:p.Ile257LeufsTer16
ENST00000426564.6:n.780del
NM_004654.3:c.768del NP_004645.2:p.Ile257LeufsTer16
XM_011531469.1:c.768del XP_011529771.1:p.Ile257LeufsTer16
XM_011531470.1:c.519+15del XP_011529772.1:n.519+15del
XM_017030078.2:c.768del XP_016885567.1:p.Ile257LeufsTer16
NM_004654.4:c.768del MANE Select NP_004645.2:p.Ile257LeufsTer16