Canonical Allele Identifier: CA2579748046
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833900_12833903del , CM000686.2:g.12833900_12833903del GRCh38
NC_000024.9:g.14945826_14945829del , CM000686.1:g.14945826_14945829del GRCh37
NC_000024.8:g.13455220_13455223del NCBI36
NG_008311.1:g.137667_137670del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5195+39_5195+42del ENSP00000498372.1:n.5195+39_5195+42del
ENST00000338981.7:c.5195+39_5195+42del MANE Select ENSP00000342812.3:n.5195+39_5195+42del
ENST00000426564.6:n.5207+39_5207+42del
NM_004654.3:c.5195+39_5195+42del NP_004645.2:n.5195+39_5195+42del
XM_011531469.1:c.5195+39_5195+42del XP_011529771.1:n.5195+39_5195+42del
XM_011531470.1:c.4961+39_4961+42del XP_011529772.1:n.4961+39_4961+42del
XM_017030078.2:c.5210+39_5210+42del XP_016885567.1:n.5210+39_5210+42del
NM_004654.4:c.5195+39_5195+42del MANE Select NP_004645.2:n.5195+39_5195+42del