Canonical Allele Identifier: CA2766240777
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735865dup , CM000686.2:g.12735865dup GRCh38
NC_000024.9:g.14847799dup , CM000686.1:g.14847799dup GRCh37
NC_000024.8:g.13357193dup NCBI36
NG_008311.1:g.39640dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.774-133dup ENSP00000498372.1:n.774-133dup
ENST00000338981.7:c.774-133dup MANE Select ENSP00000342812.3:n.774-133dup
ENST00000426564.6:n.786-133dup
NM_004654.3:c.774-133dup NP_004645.2:n.774-133dup
XM_011531469.1:c.774-133dup XP_011529771.1:n.774-133dup
XM_011531470.1:c.539+72dup XP_011529772.1:n.539+72dup
XM_017030078.2:c.774-133dup XP_016885567.1:n.774-133dup
NM_004654.4:c.774-133dup MANE Select NP_004645.2:n.774-133dup