Canonical Allele Identifier: CA2824887236
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846300_12846301dup , CM000686.2:g.12846300_12846301dup GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6569-33_6569-32dup ENSP00000498372.1:n.6569-33_6569-32dup
ENST00000338981.7:c.6569-33_6569-32dup MANE Select ENSP00000342812.3:n.6569-33_6569-32dup
ENST00000426564.6:n.6596-33_6596-32dup
NM_004654.3:c.6569-33_6569-32dup NP_004645.2:n.6569-33_6569-32dup
XM_011531469.1:c.6569-33_6569-32dup XP_011529771.1:n.6569-33_6569-32dup
XM_011531470.1:c.6335-33_6335-32dup XP_011529772.1:n.6335-33_6335-32dup
XM_017030078.2:c.6584-33_6584-32dup XP_016885567.1:n.6584-33_6584-32dup
NM_004654.4:c.6569-33_6569-32dup MANE Select NP_004645.2:n.6569-33_6569-32dup