Canonical Allele Identifier: CA1139272130
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053552968

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833981_12833984del , CM000686.2:g.12833981_12833984del GRCh38
NC_000024.9:g.14945907_14945910del , CM000686.1:g.14945907_14945910del GRCh37
NC_000024.8:g.13455301_13455304del NCBI36
NG_008311.1:g.137748_137751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5195+120_5195+123del ENSP00000498372.1:n.5195+120_5195+123del
ENST00000338981.7:c.5195+120_5195+123del MANE Select ENSP00000342812.3:n.5195+120_5195+123del
ENST00000426564.6:n.5207+120_5207+123del
NM_004654.3:c.5195+120_5195+123del NP_004645.2:n.5195+120_5195+123del
XM_011531469.1:c.5195+120_5195+123del XP_011529771.1:n.5195+120_5195+123del
XM_011531470.1:c.4961+120_4961+123del XP_011529772.1:n.4961+120_4961+123del
XM_017030078.2:c.5210+120_5210+123del XP_016885567.1:n.5210+120_5210+123del
NM_004654.4:c.5195+120_5195+123del MANE Select NP_004645.2:n.5195+120_5195+123del