Canonical Allele Identifier: CA1139279513
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12857749-G-C
gnomAD v4: Y-12857749-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857749G>C , CM000686.2:g.12857749G>C GRCh38
NC_000024.9:g.14969674G>C , CM000686.1:g.14969674G>C GRCh37
NC_000024.8:g.13479068G>C NCBI36
NG_008311.1:g.161515G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7530+88G>C ENSP00000498372.1:n.7530+88G>C
ENST00000338981.7:c.7530+88G>C MANE Select ENSP00000342812.3:n.7530+88G>C
ENST00000426564.6:n.7557+88G>C
ENST00000453031.1:c.575+88G>C
ENST00000471409.1:n.849+88G>C
NM_004654.3:c.7530+88G>C NP_004645.2:n.7530+88G>C
XM_011531469.1:c.7530+88G>C XP_011529771.1:n.7530+88G>C
XM_011531470.1:c.7296+88G>C XP_011529772.1:n.7296+88G>C
XM_017030078.2:c.7545+88G>C XP_016885567.1:n.7545+88G>C
NM_004654.4:c.7530+88G>C MANE Select NP_004645.2:n.7530+88G>C
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