Canonical Allele Identifier: CA658645130
Gene: USP9Y HGNC NCBI

Linked Data

COSMIC: COSN26769175
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12710252A>C , CM000686.2:g.12710252A>C GRCh38
NC_000024.9:g.14822185A>C , CM000686.1:g.14822185A>C GRCh37
NC_000024.8:g.13331579A>C NCBI36
NG_008311.1:g.14026A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.96+709A>C ENSP00000498372.1:n.96+709A>C
ENST00000338981.7:c.96+709A>C MANE Select ENSP00000342812.3:n.96+709A>C
ENST00000426564.6:n.108+709A>C
ENST00000493168.1:n.172+709A>C
NM_004654.3:c.96+709A>C NP_004645.2:n.96+709A>C
XM_011531469.1:c.96+709A>C XP_011529771.1:n.96+709A>C
XM_017030078.2:c.96+709A>C XP_016885567.1:n.96+709A>C
NM_004654.4:c.96+709A>C MANE Select NP_004645.2:n.96+709A>C
Search 100 bp 5'
Search 100 bp 3'