Canonical Allele Identifier: CA2766241771
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810613dup , CM000686.2:g.12810613dup GRCh38
NC_000024.9:g.14922548dup , CM000686.1:g.14922548dup GRCh37
NC_000024.8:g.13431942dup NCBI36
NG_008311.1:g.114389dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4093-59dup ENSP00000498372.1:n.4093-59dup
ENST00000338981.7:c.4093-59dup MANE Select ENSP00000342812.3:n.4093-59dup
ENST00000426564.6:n.4105-59dup
NM_004654.3:c.4093-59dup NP_004645.2:n.4093-59dup
XM_011531469.1:c.4093-59dup XP_011529771.1:n.4093-59dup
XM_011531470.1:c.3859-59dup XP_011529772.1:n.3859-59dup
XM_017030078.2:c.4108-59dup XP_016885567.1:n.4108-59dup
NM_004654.4:c.4093-59dup MANE Select NP_004645.2:n.4093-59dup
Search 100 bp 5'
Search 100 bp 3'