Canonical Allele Identifier: CA414999131
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833813T>A , CM000686.2:g.12833813T>A GRCh38
NC_000024.9:g.14945739T>A , CM000686.1:g.14945739T>A GRCh37
NC_000024.8:g.13455133T>A NCBI36
NG_008311.1:g.137580T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5147T>A ENSP00000498372.1:p.Leu1716Gln
ENST00000338981.7:c.5147T>A MANE Select ENSP00000342812.3:p.Leu1716Gln
ENST00000426564.6:n.5159T>A
NM_004654.3:c.5147T>A NP_004645.2:p.Leu1716Gln
XM_011531469.1:c.5147T>A XP_011529771.1:p.Leu1716Gln
XM_011531470.1:c.4913T>A XP_011529772.1:p.Leu1638Gln
XM_017030078.2:c.5162T>A XP_016885567.1:p.Leu1721Gln
NM_004654.4:c.5147T>A MANE Select NP_004645.2:p.Leu1716Gln