Canonical Allele Identifier: CA415007481
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778029G>A , CM000686.2:g.12778029G>A GRCh38
NC_000024.9:g.14889963G>A , CM000686.1:g.14889963G>A GRCh37
NC_000024.8:g.13399357G>A NCBI36
NG_008311.1:g.81804G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2650G>A ENSP00000498372.1:p.Gly884Ser
ENST00000338981.7:c.2650G>A MANE Select ENSP00000342812.3:p.Gly884Ser
ENST00000426564.6:n.2662G>A
NM_004654.3:c.2650G>A NP_004645.2:p.Gly884Ser
XM_011531469.1:c.2650G>A XP_011529771.1:p.Gly884Ser
XM_011531470.1:c.2416G>A XP_011529772.1:p.Gly806Ser
XM_017030078.2:c.2665G>A XP_016885567.1:p.Gly889Ser
NM_004654.4:c.2650G>A MANE Select NP_004645.2:p.Gly884Ser