Canonical Allele Identifier: CA1139183277
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12778366-G-A
gnomAD v4: Y-12778366-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778366G>A , CM000686.2:g.12778366G>A GRCh38
NC_000024.9:g.14890300G>A , CM000686.1:g.14890300G>A GRCh37
NC_000024.8:g.13399694G>A NCBI36
NG_008311.1:g.82141G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2880+107G>A ENSP00000498372.1:n.2880+107G>A
ENST00000338981.7:c.2880+107G>A MANE Select ENSP00000342812.3:n.2880+107G>A
ENST00000426564.6:n.2892+107G>A
NM_004654.3:c.2880+107G>A NP_004645.2:n.2880+107G>A
XM_011531469.1:c.2880+107G>A XP_011529771.1:n.2880+107G>A
XM_011531470.1:c.2646+107G>A XP_011529772.1:n.2646+107G>A
XM_017030078.2:c.2895+107G>A XP_016885567.1:n.2895+107G>A
NM_004654.4:c.2880+107G>A MANE Select NP_004645.2:n.2880+107G>A
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