Canonical Allele Identifier: CA2470560465
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833900G= , CM000686.2:g.12833900G= GRCh38
NC_000024.9:g.14945826G= , CM000686.1:g.14945826G= GRCh37
NC_000024.8:g.13455220G= NCBI36
NG_008311.1:g.137667G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5195+39G= ENSP00000498372.1:n.5195+39G=
ENST00000338981.7:c.5195+39G= MANE Select ENSP00000342812.3:n.5195+39G=
ENST00000426564.6:n.5207+39G=
NM_004654.3:c.5195+39G= NP_004645.2:n.5195+39G=
XM_011531469.1:c.5195+39G= XP_011529771.1:n.5195+39G=
XM_011531470.1:c.4961+39G= XP_011529772.1:n.4961+39G=
XM_017030078.2:c.5210+39G= XP_016885567.1:n.5210+39G=
NM_004654.4:c.5195+39G= MANE Select NP_004645.2:n.5195+39G=
Search 100 bp 5'
Search 100 bp 3'