Canonical Allele Identifier: CA2766241285
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778044_12778045del , CM000686.2:g.12778044_12778045del GRCh38
NC_000024.9:g.14889978_14889979del , CM000686.1:g.14889978_14889979del GRCh37
NC_000024.8:g.13399372_13399373del NCBI36
NG_008311.1:g.81819_81820del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2665_2666del ENSP00000498372.1:p.Leu889TyrfsTer12
ENST00000338981.7:c.2665_2666del MANE Select ENSP00000342812.3:p.Leu889TyrfsTer12
ENST00000426564.6:n.2677_2678del
NM_004654.3:c.2665_2666del NP_004645.2:p.Leu889TyrfsTer12
XM_011531469.1:c.2665_2666del XP_011529771.1:p.Leu889TyrfsTer12
XM_011531470.1:c.2431_2432del XP_011529772.1:p.Leu811TyrfsTer12
XM_017030078.2:c.2680_2681del XP_016885567.1:p.Leu894TyrfsTer12
NM_004654.4:c.2665_2666del MANE Select NP_004645.2:p.Leu889TyrfsTer12