Canonical Allele Identifier: CA414980722
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720696T>G , CM000686.2:g.12720696T>G GRCh38
NC_000024.9:g.14832629T>G , CM000686.1:g.14832629T>G GRCh37
NC_000024.8:g.13342023T>G NCBI36
NG_008311.1:g.24470T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.204T>G ENSP00000498372.1:p.Phe68Leu
ENST00000338981.7:c.204T>G MANE Select ENSP00000342812.3:p.Phe68Leu
ENST00000426564.6:n.216T>G
ENST00000493168.1:n.280T>G
NM_004654.3:c.204T>G NP_004645.2:p.Phe68Leu
XM_011531469.1:c.204T>G XP_011529771.1:p.Phe68Leu
XM_011531470.1:c.-31T>G XP_011529772.1:n.-31T>G
XM_017030078.2:c.204T>G XP_016885567.1:p.Phe68Leu
NM_004654.4:c.204T>G MANE Select NP_004645.2:p.Phe68Leu