Canonical Allele Identifier: CA2527798157
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12856600_12856601del , CM000686.2:g.12856600_12856601del GRCh38
NC_000024.9:g.14968525_14968526del , CM000686.1:g.14968525_14968526del GRCh37
NC_000024.8:g.13477919_13477920del NCBI36
NG_008311.1:g.160366_160367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7222-33_7222-32del ENSP00000498372.1:n.7222-33_7222-32del
ENST00000338981.7:c.7222-33_7222-32del MANE Select ENSP00000342812.3:n.7222-33_7222-32del
ENST00000426564.6:n.7249-33_7249-32del
ENST00000453031.1:c.267-33_267-32del
NM_004654.3:c.7222-33_7222-32del NP_004645.2:n.7222-33_7222-32del
XM_011531469.1:c.7222-33_7222-32del XP_011529771.1:n.7222-33_7222-32del
XM_011531470.1:c.6988-33_6988-32del XP_011529772.1:n.6988-33_6988-32del
XM_017030078.2:c.7237-33_7237-32del XP_016885567.1:n.7237-33_7237-32del
NM_004654.4:c.7222-33_7222-32del MANE Select NP_004645.2:n.7222-33_7222-32del