Canonical Allele Identifier: CA2824884730
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735581dup , CM000686.2:g.12735581dup GRCh38
NC_000024.9:g.14847515dup , CM000686.1:g.14847515dup GRCh37
NC_000024.8:g.13356909dup NCBI36
NG_008311.1:g.39356dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.658-31dup ENSP00000498372.1:n.658-31dup
ENST00000338981.7:c.658-31dup MANE Select ENSP00000342812.3:n.658-31dup
ENST00000426564.6:n.670-31dup
NM_004654.3:c.658-31dup NP_004645.2:n.658-31dup
XM_011531469.1:c.658-31dup XP_011529771.1:n.658-31dup
XM_011531470.1:c.424-31dup XP_011529772.1:n.424-31dup
XM_017030078.2:c.658-31dup XP_016885567.1:n.658-31dup
NM_004654.4:c.658-31dup MANE Select NP_004645.2:n.658-31dup