Canonical Allele Identifier: CA2470554869
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12726767C= , CM000686.2:g.12726767C= GRCh38
NC_000024.9:g.14838700C= , CM000686.1:g.14838700C= GRCh37
NC_000024.8:g.13348094C= NCBI36
NG_008311.1:g.30541C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.631C= ENSP00000498372.1:p.Arg211=
ENST00000338981.7:c.631C= MANE Select ENSP00000342812.3:p.Arg211=
ENST00000426564.6:n.643C=
NM_004654.3:c.631C= NP_004645.2:p.Arg211=
XM_011531469.1:c.631C= XP_011529771.1:p.Arg211=
XM_011531470.1:c.397C= XP_011529772.1:p.Arg133=
XM_017030078.2:c.631C= XP_016885567.1:p.Arg211=
NM_004654.4:c.631C= MANE Select NP_004645.2:p.Arg211=