Canonical Allele Identifier: CA2766240752
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735676del , CM000686.2:g.12735676del GRCh38
NC_000024.9:g.14847610del , CM000686.1:g.14847610del GRCh37
NC_000024.8:g.13357004del NCBI36
NG_008311.1:g.39451del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.722del ENSP00000498372.1:p.Arg241LeufsTer8
ENST00000338981.7:c.722del MANE Select ENSP00000342812.3:p.Arg241LeufsTer8
ENST00000426564.6:n.734del
NM_004654.3:c.722del NP_004645.2:p.Arg241LeufsTer8
XM_011531469.1:c.722del XP_011529771.1:p.Arg241LeufsTer8
XM_011531470.1:c.488del XP_011529772.1:p.Arg163LeufsTer8
XM_017030078.2:c.722del XP_016885567.1:p.Arg241LeufsTer8
NM_004654.4:c.722del MANE Select NP_004645.2:p.Arg241LeufsTer8
Search 100 bp 5'
Search 100 bp 3'