Canonical Allele Identifier: CA2470560458
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833804G= , CM000686.2:g.12833804G= GRCh38
NC_000024.9:g.14945730G= , CM000686.1:g.14945730G= GRCh37
NC_000024.8:g.13455124G= NCBI36
NG_008311.1:g.137571G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.5138G= ENSP00000498372.1:p.Ser1713=
ENST00000338981.7:c.5138G= MANE Select ENSP00000342812.3:p.Ser1713=
ENST00000426564.6:n.5150G=
NM_004654.3:c.5138G= NP_004645.2:p.Ser1713=
XM_011531469.1:c.5138G= XP_011529771.1:p.Ser1713=
XM_011531470.1:c.4904G= XP_011529772.1:p.Ser1635=
XM_017030078.2:c.5153G= XP_016885567.1:p.Ser1718=
NM_004654.4:c.5138G= MANE Select NP_004645.2:p.Ser1713=