Canonical Allele Identifier: CA415007531
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846387T>A , CM000686.2:g.12846387T>A GRCh38
NC_000024.9:g.14958312T>A , CM000686.1:g.14958312T>A GRCh37
NC_000024.8:g.13467706T>A NCBI36
NG_008311.1:g.150153T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6623T>A ENSP00000498372.1:p.Leu2208His
ENST00000338981.7:c.6623T>A MANE Select ENSP00000342812.3:p.Leu2208His
ENST00000426564.6:n.6650T>A
NM_004654.3:c.6623T>A NP_004645.2:p.Leu2208His
XM_011531469.1:c.6623T>A XP_011529771.1:p.Leu2208His
XM_011531470.1:c.6389T>A XP_011529772.1:p.Leu2130His
XM_017030078.2:c.6638T>A XP_016885567.1:p.Leu2213His
NM_004654.4:c.6623T>A MANE Select NP_004645.2:p.Leu2208His