Canonical Allele Identifier: CA2766241294
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778317_12778320del , CM000686.2:g.12778317_12778320del GRCh38
NC_000024.9:g.14890251_14890254del , CM000686.1:g.14890251_14890254del GRCh37
NC_000024.8:g.13399645_13399648del NCBI36
NG_008311.1:g.82092_82095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2880+58_2880+61del ENSP00000498372.1:n.2880+58_2880+61del
ENST00000338981.7:c.2880+58_2880+61del MANE Select ENSP00000342812.3:n.2880+58_2880+61del
ENST00000426564.6:n.2892+58_2892+61del
NM_004654.3:c.2880+58_2880+61del NP_004645.2:n.2880+58_2880+61del
XM_011531469.1:c.2880+58_2880+61del XP_011529771.1:n.2880+58_2880+61del
XM_011531470.1:c.2646+58_2646+61del XP_011529772.1:n.2646+58_2646+61del
XM_017030078.2:c.2895+58_2895+61del XP_016885567.1:n.2895+58_2895+61del
NM_004654.4:c.2880+58_2880+61del MANE Select NP_004645.2:n.2880+58_2880+61del