Canonical Allele Identifier: CA2766240773
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735848del , CM000686.2:g.12735848del GRCh38
NC_000024.9:g.14847782del , CM000686.1:g.14847782del GRCh37
NC_000024.8:g.13357176del NCBI36
NG_008311.1:g.39623del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.773+121del ENSP00000498372.1:n.773+121del
ENST00000338981.7:c.773+121del MANE Select ENSP00000342812.3:n.773+121del
ENST00000426564.6:n.785+121del
NM_004654.3:c.773+121del NP_004645.2:n.773+121del
XM_011531469.1:c.773+121del XP_011529771.1:n.773+121del
XM_011531470.1:c.539+55del XP_011529772.1:n.539+55del
XM_017030078.2:c.773+121del XP_016885567.1:n.773+121del
NM_004654.4:c.773+121del MANE Select NP_004645.2:n.773+121del