Canonical Allele Identifier: CA415009211
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778224A>G , CM000686.2:g.12778224A>G GRCh38
NC_000024.9:g.14890158A>G , CM000686.1:g.14890158A>G GRCh37
NC_000024.8:g.13399552A>G NCBI36
NG_008311.1:g.81999A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2845A>G ENSP00000498372.1:p.Lys949Glu
ENST00000338981.7:c.2845A>G MANE Select ENSP00000342812.3:p.Lys949Glu
ENST00000426564.6:n.2857A>G
NM_004654.3:c.2845A>G NP_004645.2:p.Lys949Glu
XM_011531469.1:c.2845A>G XP_011529771.1:p.Lys949Glu
XM_011531470.1:c.2611A>G XP_011529772.1:p.Lys871Glu
XM_017030078.2:c.2860A>G XP_016885567.1:p.Lys954Glu
NM_004654.4:c.2845A>G MANE Select NP_004645.2:p.Lys949Glu