Canonical Allele Identifier: CA414983421
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790413C>G , CM000686.2:g.12790413C>G GRCh38
NC_000024.9:g.14902346C>G , CM000686.1:g.14902346C>G GRCh37
NC_000024.8:g.13411740C>G NCBI36
NG_008311.1:g.94187C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3568C>G ENSP00000498372.1:p.Gln1190Glu
ENST00000338981.7:c.3568C>G MANE Select ENSP00000342812.3:p.Gln1190Glu
ENST00000426564.6:n.3580C>G
NM_004654.3:c.3568C>G NP_004645.2:p.Gln1190Glu
XM_011531469.1:c.3568C>G XP_011529771.1:p.Gln1190Glu
XM_011531470.1:c.3334C>G XP_011529772.1:p.Gln1112Glu
XM_017030078.2:c.3583C>G XP_016885567.1:p.Gln1195Glu
NM_004654.4:c.3568C>G MANE Select NP_004645.2:p.Gln1190Glu