Canonical Allele Identifier: CA2470553961
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12710237_12710238delinsTA , CM000686.2:g.12710237_12710238delinsTA GRCh38
NC_000024.9:g.14822170_14822171delinsTA , CM000686.1:g.14822170_14822171delinsTA GRCh37
NC_000024.8:g.13331564_13331565delinsTA NCBI36
NG_008311.1:g.14011_14012delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.96+694_96+695delinsTA ENSP00000498372.1:n.96+694_96+695delinsTA
ENST00000338981.7:c.96+694_96+695delinsTA MANE Select ENSP00000342812.3:n.96+694_96+695delinsTA
ENST00000426564.6:n.108+694_108+695delinsTA
ENST00000493168.1:n.172+694_172+695delinsTA
NM_004654.3:c.96+694_96+695delinsTA NP_004645.2:n.96+694_96+695delinsTA
XM_011531469.1:c.96+694_96+695delinsTA XP_011529771.1:n.96+694_96+695delinsTA
XM_017030078.2:c.96+694_96+695delinsTA XP_016885567.1:n.96+694_96+695delinsTA
NM_004654.4:c.96+694_96+695delinsTA MANE Select NP_004645.2:n.96+694_96+695delinsTA