Canonical Allele Identifier: CA2470558126
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790478C= , CM000686.2:g.12790478C= GRCh38
NC_000024.9:g.14902411C= , CM000686.1:g.14902411C= GRCh37
NC_000024.8:g.13411805C= NCBI36
NG_008311.1:g.94252C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3633C= ENSP00000498372.1:p.Ser1211=
ENST00000338981.7:c.3633C= MANE Select ENSP00000342812.3:p.Ser1211=
ENST00000426564.6:n.3645C=
NM_004654.3:c.3633C= NP_004645.2:p.Ser1211=
XM_011531469.1:c.3633C= XP_011529771.1:p.Ser1211=
XM_011531470.1:c.3399C= XP_011529772.1:p.Ser1133=
XM_017030078.2:c.3648C= XP_016885567.1:p.Ser1216=
NM_004654.4:c.3633C= MANE Select NP_004645.2:p.Ser1211=