Canonical Allele Identifier: CA2766242288
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846284_12846291del , CM000686.2:g.12846284_12846291del GRCh38
NC_000024.9:g.14958209_14958216del , CM000686.1:g.14958209_14958216del GRCh37
NC_000024.8:g.13467603_13467610del NCBI36
NG_008311.1:g.150050_150057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6569-49_6569-42del ENSP00000498372.1:n.6569-49_6569-42del
ENST00000338981.7:c.6569-49_6569-42del MANE Select ENSP00000342812.3:n.6569-49_6569-42del
ENST00000426564.6:n.6596-49_6596-42del
NM_004654.3:c.6569-49_6569-42del NP_004645.2:n.6569-49_6569-42del
XM_011531469.1:c.6569-49_6569-42del XP_011529771.1:n.6569-49_6569-42del
XM_011531470.1:c.6335-49_6335-42del XP_011529772.1:n.6335-49_6335-42del
XM_017030078.2:c.6584-49_6584-42del XP_016885567.1:n.6584-49_6584-42del
NM_004654.4:c.6569-49_6569-42del MANE Select NP_004645.2:n.6569-49_6569-42del