Canonical Allele Identifier: CA1139263912
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053529286

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810613del , CM000686.2:g.12810613del GRCh38
NC_000024.9:g.14922548del , CM000686.1:g.14922548del GRCh37
NC_000024.8:g.13431942del NCBI36
NG_008311.1:g.114389del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4093-59del ENSP00000498372.1:n.4093-59del
ENST00000338981.7:c.4093-59del MANE Select ENSP00000342812.3:n.4093-59del
ENST00000426564.6:n.4105-59del
NM_004654.3:c.4093-59del NP_004645.2:n.4093-59del
XM_011531469.1:c.4093-59del XP_011529771.1:n.4093-59del
XM_011531470.1:c.3859-59del XP_011529772.1:n.3859-59del
XM_017030078.2:c.4108-59del XP_016885567.1:n.4108-59del
NM_004654.4:c.4093-59del MANE Select NP_004645.2:n.4093-59del