Canonical Allele Identifier: CA2502670597
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846328del , CM000686.2:g.12846328del GRCh38
NC_000024.9:g.14958253del , CM000686.1:g.14958253del GRCh37
NC_000024.8:g.13467647del NCBI36
NG_008311.1:g.150094del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.6569-5del ENSP00000498372.1:n.6569-5del
ENST00000338981.7:c.6569-5del MANE Select ENSP00000342812.3:n.6569-5del
ENST00000426564.6:n.6596-5del
NM_004654.3:c.6569-5del NP_004645.2:n.6569-5del
XM_011531469.1:c.6569-5del XP_011529771.1:n.6569-5del
XM_011531470.1:c.6335-5del XP_011529772.1:n.6335-5del
XM_017030078.2:c.6584-5del XP_016885567.1:n.6584-5del
NM_004654.4:c.6569-5del MANE Select NP_004645.2:n.6569-5del