Canonical Allele Identifier: CA1139183196
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12777987-A-C
gnomAD v4: Y-12777987-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777987A>C , CM000686.2:g.12777987A>C GRCh38
NC_000024.9:g.14889921A>C , CM000686.1:g.14889921A>C GRCh37
NC_000024.8:g.13399315A>C NCBI36
NG_008311.1:g.81762A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2640-32A>C ENSP00000498372.1:n.2640-32A>C
ENST00000338981.7:c.2640-32A>C MANE Select ENSP00000342812.3:n.2640-32A>C
ENST00000426564.6:n.2652-32A>C
NM_004654.3:c.2640-32A>C NP_004645.2:n.2640-32A>C
XM_011531469.1:c.2640-32A>C XP_011529771.1:n.2640-32A>C
XM_011531470.1:c.2406-32A>C XP_011529772.1:n.2406-32A>C
XM_017030078.2:c.2655-32A>C XP_016885567.1:n.2655-32A>C
NM_004654.4:c.2640-32A>C MANE Select NP_004645.2:n.2640-32A>C
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