Canonical Allele Identifier: CA2824887238
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846292_12846293insC , CM000686.2:g.12846292_12846293insC GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6569-41_6569-40insC ENSP00000498372.1:n.6569-41_6569-40insC
ENST00000338981.7:c.6569-41_6569-40insC MANE Select ENSP00000342812.3:n.6569-41_6569-40insC
ENST00000426564.6:n.6596-41_6596-40insC
NM_004654.3:c.6569-41_6569-40insC NP_004645.2:n.6569-41_6569-40insC
XM_011531469.1:c.6569-41_6569-40insC XP_011529771.1:n.6569-41_6569-40insC
XM_011531470.1:c.6335-41_6335-40insC XP_011529772.1:n.6335-41_6335-40insC
XM_017030078.2:c.6584-41_6584-40insC XP_016885567.1:n.6584-41_6584-40insC
NM_004654.4:c.6569-41_6569-40insC MANE Select NP_004645.2:n.6569-41_6569-40insC