Canonical Allele Identifier: CA2513369147
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735790_12735792del , CM000686.2:g.12735790_12735792del GRCh38
NC_000024.9:g.14847724_14847726del , CM000686.1:g.14847724_14847726del GRCh37
NC_000024.8:g.13357118_13357120del NCBI36
NG_008311.1:g.39565_39567del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.773+63_773+65del ENSP00000498372.1:n.773+63_773+65del
ENST00000338981.7:c.773+63_773+65del MANE Select ENSP00000342812.3:n.773+63_773+65del
ENST00000426564.6:n.785+63_785+65del
NM_004654.3:c.773+63_773+65del NP_004645.2:n.773+63_773+65del
XM_011531469.1:c.773+63_773+65del XP_011529771.1:n.773+63_773+65del
XM_011531470.1:c.536_538del XP_011529772.1:p.Ile179del
XM_017030078.2:c.773+63_773+65del XP_016885567.1:n.773+63_773+65del
NM_004654.4:c.773+63_773+65del MANE Select NP_004645.2:n.773+63_773+65del