Canonical Allele Identifier: CA2470559199
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810736A= , CM000686.2:g.12810736A= GRCh38
NC_000024.9:g.14922671A= , CM000686.1:g.14922671A= GRCh37
NC_000024.8:g.13432065A= NCBI36
NG_008311.1:g.114512A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4157A= ENSP00000498372.1:p.Asn1386=
ENST00000338981.7:c.4157A= MANE Select ENSP00000342812.3:p.Asn1386=
ENST00000426564.6:n.4169A=
NM_004654.3:c.4157A= NP_004645.2:p.Asn1386=
XM_011531469.1:c.4157A= XP_011529771.1:p.Asn1386=
XM_011531470.1:c.3923A= XP_011529772.1:p.Asn1308=
XM_017030078.2:c.4172A= XP_016885567.1:p.Asn1391=
NM_004654.4:c.4157A= MANE Select NP_004645.2:p.Asn1386=