Canonical Allele Identifier: CA2470554870
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12726768G= , CM000686.2:g.12726768G= GRCh38
NC_000024.9:g.14838701G= , CM000686.1:g.14838701G= GRCh37
NC_000024.8:g.13348095G= NCBI36
NG_008311.1:g.30542G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.632G= ENSP00000498372.1:p.Arg211=
ENST00000338981.7:c.632G= MANE Select ENSP00000342812.3:p.Arg211=
ENST00000426564.6:n.644G=
NM_004654.3:c.632G= NP_004645.2:p.Arg211=
XM_011531469.1:c.632G= XP_011529771.1:p.Arg211=
XM_011531470.1:c.398G= XP_011529772.1:p.Arg133=
XM_017030078.2:c.632G= XP_016885567.1:p.Arg211=
NM_004654.4:c.632G= MANE Select NP_004645.2:p.Arg211=