Canonical Allele Identifier: CA2824887235
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846301_12846302insTTTTTTTTTTTTTTT , CM000686.2:g.12846301_12846302insTTTTTTTTTTTTTTT GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6569-32_6569-31insTTTTTTTTTTTTTTT ENSP00000498372.1:n.6569-32_6569-31insTTTTTTTTTTTTTTT
ENST00000338981.7:c.6569-32_6569-31insTTTTTTTTTTTTTTT MANE Select ENSP00000342812.3:n.6569-32_6569-31insTTTTTTTTTTTTTTT
ENST00000426564.6:n.6596-32_6596-31insTTTTTTTTTTTTTTT
NM_004654.3:c.6569-32_6569-31insTTTTTTTTTTTTTTT NP_004645.2:n.6569-32_6569-31insTTTTTTTTTTTTTTT
XM_011531469.1:c.6569-32_6569-31insTTTTTTTTTTTTTTT XP_011529771.1:n.6569-32_6569-31insTTTTTTTTTTTTTTT
XM_011531470.1:c.6335-32_6335-31insTTTTTTTTTTTTTTT XP_011529772.1:n.6335-32_6335-31insTTTTTTTTTTTTTTT
XM_017030078.2:c.6584-32_6584-31insTTTTTTTTTTTTTTT XP_016885567.1:n.6584-32_6584-31insTTTTTTTTTTTTTTT
NM_004654.4:c.6569-32_6569-31insTTTTTTTTTTTTTTT MANE Select NP_004645.2:n.6569-32_6569-31insTTTTTTTTTTTTTTT