Canonical Allele Identifier: CA337718165
Gene: USP9Y HGNC NCBI
TTTY15 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12665429A>G
GRCh37 chrY:g.14777360A>G
gnomAD v3:
Y:12665429 A / G
gnomAD v4:
chrY-12665429-A-G
Joint Max Group AF 0.59638917 (AFR)
Genomes Max Group AF 0.59638917 (AFR)
dbSNP:
9786605
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12665429A>G , CM000686.2:g.12665429A>G GRCh38
NC_000024.9:g.14777360A>G , CM000686.1:g.14777360A>G GRCh37
NC_000024.8:g.13286754A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000417071.1:n.217+743A>G
ENST00000440408.5:n.420+743A>G
ENST00000457658.6:n.1051+743A>G (USP9Y)
ENST00000651177.1:c.-201+743A>G (USP9Y) ENSP00000498372.1:n.-201+743A>G
NR_001545.2:n.387+743A>G (TTTY15)
NR_001545.3:n.402+743A>G (TTTY15)
NR_174085.1:n.355+2723A>G (TTTY15)
NR_174086.1:n.355+2723A>G (TTTY15)
NR_174087.1:n.402+743A>G (TTTY15)
NR_174088.1:n.402+743A>G (TTTY15)
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