Canonical Allele Identifier: CA2579748037
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833624_12833626del , CM000686.2:g.12833624_12833626del GRCh38
NC_000024.9:g.14945550_14945552del , CM000686.1:g.14945550_14945552del GRCh37
NC_000024.8:g.13454944_13454946del NCBI36
NG_008311.1:g.137391_137393del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.5022-64_5022-62del ENSP00000498372.1:n.5022-64_5022-62del
ENST00000338981.7:c.5022-64_5022-62del MANE Select ENSP00000342812.3:n.5022-64_5022-62del
ENST00000426564.6:n.5034-64_5034-62del
NM_004654.3:c.5022-64_5022-62del NP_004645.2:n.5022-64_5022-62del
XM_011531469.1:c.5022-64_5022-62del XP_011529771.1:n.5022-64_5022-62del
XM_011531470.1:c.4788-64_4788-62del XP_011529772.1:n.4788-64_4788-62del
XM_017030078.2:c.5037-64_5037-62del XP_016885567.1:n.5037-64_5037-62del
NM_004654.4:c.5022-64_5022-62del MANE Select NP_004645.2:n.5022-64_5022-62del