Canonical Allele Identifier: CA1139279523
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12857789-C-G
gnomAD v4: Y-12857789-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857789C>G , CM000686.2:g.12857789C>G GRCh38
NC_000024.9:g.14969714C>G , CM000686.1:g.14969714C>G GRCh37
NC_000024.8:g.13479108C>G NCBI36
NG_008311.1:g.161555C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7530+128C>G ENSP00000498372.1:n.7530+128C>G
ENST00000338981.7:c.7530+128C>G MANE Select ENSP00000342812.3:n.7530+128C>G
ENST00000426564.6:n.7557+128C>G
ENST00000453031.1:c.575+128C>G
ENST00000471409.1:n.849+128C>G
NM_004654.3:c.7530+128C>G NP_004645.2:n.7530+128C>G
XM_011531469.1:c.7530+128C>G XP_011529771.1:n.7530+128C>G
XM_011531470.1:c.7296+128C>G XP_011529772.1:n.7296+128C>G
XM_017030078.2:c.7545+128C>G XP_016885567.1:n.7545+128C>G
NM_004654.4:c.7530+128C>G MANE Select NP_004645.2:n.7530+128C>G
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