Canonical Allele Identifier: CA2470558124
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790420C= , CM000686.2:g.12790420C= GRCh38
NC_000024.9:g.14902353C= , CM000686.1:g.14902353C= GRCh37
NC_000024.8:g.13411747C= NCBI36
NG_008311.1:g.94194C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3575C= ENSP00000498372.1:p.Thr1192=
ENST00000338981.7:c.3575C= MANE Select ENSP00000342812.3:p.Thr1192=
ENST00000426564.6:n.3587C=
NM_004654.3:c.3575C= NP_004645.2:p.Thr1192=
XM_011531469.1:c.3575C= XP_011529771.1:p.Thr1192=
XM_011531470.1:c.3341C= XP_011529772.1:p.Thr1114=
XM_017030078.2:c.3590C= XP_016885567.1:p.Thr1197=
NM_004654.4:c.3575C= MANE Select NP_004645.2:p.Thr1192=