Canonical Allele Identifier: CA10573012
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs7067496

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720687G>T , CM000686.2:g.12720687G>T GRCh38
NC_000024.9:g.14832620G>T , CM000686.1:g.14832620G>T GRCh37
NC_000024.8:g.13342014G>T NCBI36
NG_008311.1:g.24461G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.195G>T ENSP00000498372.1:p.Glu65Asp
ENST00000338981.7:c.195G>T MANE Select ENSP00000342812.3:p.Glu65Asp
ENST00000426564.6:n.207G>T
ENST00000493168.1:n.271G>T
NM_004654.3:c.195G>T NP_004645.2:p.Glu65Asp
XM_011531469.1:c.195G>T XP_011529771.1:p.Glu65Asp
XM_011531470.1:c.-40G>T XP_011529772.1:n.-40G>T
XM_017030078.2:c.195G>T XP_016885567.1:p.Glu65Asp
NM_004654.4:c.195G>T MANE Select NP_004645.2:p.Glu65Asp