Canonical Allele Identifier: CA2470559177
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810478G= , CM000686.2:g.12810478G= GRCh38
NC_000024.9:g.14922413G= , CM000686.1:g.14922413G= GRCh37
NC_000024.8:g.13431807G= NCBI36
NG_008311.1:g.114254G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4092+191G= ENSP00000498372.1:n.4092+191G=
ENST00000338981.7:c.4092+191G= MANE Select ENSP00000342812.3:n.4092+191G=
ENST00000426564.6:n.4104+191G=
NM_004654.3:c.4092+191G= NP_004645.2:n.4092+191G=
XM_011531469.1:c.4092+191G= XP_011529771.1:n.4092+191G=
XM_011531470.1:c.3858+191G= XP_011529772.1:n.3858+191G=
XM_017030078.2:c.4107+191G= XP_016885567.1:n.4107+191G=
NM_004654.4:c.4092+191G= MANE Select NP_004645.2:n.4092+191G=
Search 100 bp 5'
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