Canonical Allele Identifier: CA2766242293
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846347dup , CM000686.2:g.12846347dup GRCh38
NC_000024.9:g.14958272dup , CM000686.1:g.14958272dup GRCh37
NC_000024.8:g.13467666dup NCBI36
NG_008311.1:g.150113dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6583dup ENSP00000498372.1:p.Thr2195AsnfsTer?
ENST00000338981.7:c.6583dup MANE Select ENSP00000342812.3:p.Thr2195AsnfsTer?
ENST00000426564.6:n.6610dup
NM_004654.3:c.6583dup NP_004645.2:p.Thr2195AsnfsTer?
XM_011531469.1:c.6583dup XP_011529771.1:p.Thr2195AsnfsTer?
XM_011531470.1:c.6349dup XP_011529772.1:p.Thr2117AsnfsTer?
XM_017030078.2:c.6598dup XP_016885567.1:p.Thr2200AsnfsTer?
NM_004654.4:c.6583dup MANE Select NP_004645.2:p.Thr2195AsnfsTer?