Canonical Allele Identifier: CA1139170112
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053451032

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735793_12735797del , CM000686.2:g.12735793_12735797del GRCh38
NC_000024.9:g.14847727_14847731del , CM000686.1:g.14847727_14847731del GRCh37
NC_000024.8:g.13357121_13357125del NCBI36
NG_008311.1:g.39568_39572del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.773+66_773+70del ENSP00000498372.1:n.773+66_773+70del
ENST00000338981.7:c.773+66_773+70del MANE Select ENSP00000342812.3:n.773+66_773+70del
ENST00000426564.6:n.785+66_785+70del
NM_004654.3:c.773+66_773+70del NP_004645.2:n.773+66_773+70del
XM_011531469.1:c.773+66_773+70del XP_011529771.1:n.773+66_773+70del
XM_011531470.1:c.539_539+4del
XM_017030078.2:c.773+66_773+70del XP_016885567.1:n.773+66_773+70del
NM_004654.4:c.773+66_773+70del MANE Select NP_004645.2:n.773+66_773+70del