Canonical Allele Identifier: CA2568533411
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12812751_12812752insGAC , CM000686.2:g.12812751_12812752insGAC GRCh38
NC_000024.9:g.14924686_14924687insGAC , CM000686.1:g.14924686_14924687insGAC GRCh37
NC_000024.8:g.13434080_13434081insGAC NCBI36
NG_008311.1:g.116527_116528insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4387-79_4387-78insGAC ENSP00000498372.1:n.4387-79_4387-78insGAC
ENST00000338981.7:c.4387-79_4387-78insGAC MANE Select ENSP00000342812.3:n.4387-79_4387-78insGAC
ENST00000426564.6:n.4399-79_4399-78insGAC
NM_004654.3:c.4387-79_4387-78insGAC NP_004645.2:n.4387-79_4387-78insGAC
XM_011531469.1:c.4387-79_4387-78insGAC XP_011529771.1:n.4387-79_4387-78insGAC
XM_011531470.1:c.4153-79_4153-78insGAC XP_011529772.1:n.4153-79_4153-78insGAC
XM_017030078.2:c.4402-79_4402-78insGAC XP_016885567.1:n.4402-79_4402-78insGAC
NM_004654.4:c.4387-79_4387-78insGAC MANE Select NP_004645.2:n.4387-79_4387-78insGAC