Canonical Allele Identifier: CA2470558130
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790485G= , CM000686.2:g.12790485G= GRCh38
NC_000024.9:g.14902418G= , CM000686.1:g.14902418G= GRCh37
NC_000024.8:g.13411812G= NCBI36
NG_008311.1:g.94259G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3640G= ENSP00000498372.1:p.Val1214=
ENST00000338981.7:c.3640G= MANE Select ENSP00000342812.3:p.Val1214=
ENST00000426564.6:n.3652G=
NM_004654.3:c.3640G= NP_004645.2:p.Val1214=
XM_011531469.1:c.3640G= XP_011529771.1:p.Val1214=
XM_011531470.1:c.3406G= XP_011529772.1:p.Val1136=
XM_017030078.2:c.3655G= XP_016885567.1:p.Val1219=
NM_004654.4:c.3640G= MANE Select NP_004645.2:p.Val1214=