Canonical Allele Identifier: CA1139162923
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12710109-G-A
gnomAD v4: Y-12710109-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12710109G>A , CM000686.2:g.12710109G>A GRCh38
NC_000024.9:g.14822042G>A , CM000686.1:g.14822042G>A GRCh37
NC_000024.8:g.13331436G>A NCBI36
NG_008311.1:g.13883G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.96+566G>A ENSP00000498372.1:n.96+566G>A
ENST00000338981.7:c.96+566G>A MANE Select ENSP00000342812.3:n.96+566G>A
ENST00000426564.6:n.108+566G>A
ENST00000493168.1:n.172+566G>A
NM_004654.3:c.96+566G>A NP_004645.2:n.96+566G>A
XM_011531469.1:c.96+566G>A XP_011529771.1:n.96+566G>A
XM_017030078.2:c.96+566G>A XP_016885567.1:n.96+566G>A
NM_004654.4:c.96+566G>A MANE Select NP_004645.2:n.96+566G>A