Canonical Allele Identifier: CA414999161
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833822C>T , CM000686.2:g.12833822C>T GRCh38
NC_000024.9:g.14945748C>T , CM000686.1:g.14945748C>T GRCh37
NC_000024.8:g.13455142C>T NCBI36
NG_008311.1:g.137589C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5156C>T ENSP00000498372.1:p.Ser1719Phe
ENST00000338981.7:c.5156C>T MANE Select ENSP00000342812.3:p.Ser1719Phe
ENST00000426564.6:n.5168C>T
NM_004654.3:c.5156C>T NP_004645.2:p.Ser1719Phe
XM_011531469.1:c.5156C>T XP_011529771.1:p.Ser1719Phe
XM_011531470.1:c.4922C>T XP_011529772.1:p.Ser1641Phe
XM_017030078.2:c.5171C>T XP_016885567.1:p.Ser1724Phe
NM_004654.4:c.5156C>T MANE Select NP_004645.2:p.Ser1719Phe