Canonical Allele Identifier: CA10573232
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12786229G>A
GRCh37 chrY:g.14898163G>A
gnomAD v2:
Y:14898163 G / A
gnomAD v3:
Y:12786229 G / A
gnomAD v4:
chrY-12786229-G-A
Joint Max Group AF 0.04193738 (MID)
Genomes Max Group AF 0.01339056 (AMR)
Exomes Max Group AF 0.04379024 (MID)
dbSNP:
20320
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12786229G>A , CM000686.2:g.12786229G>A GRCh38
NC_000024.9:g.14898163G>A , CM000686.1:g.14898163G>A GRCh37
NC_000024.8:g.13407557G>A NCBI36
NG_008311.1:g.90004G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3178G>A ENSP00000498372.1:p.Ala1060Thr
ENST00000338981.7:c.3178G>A MANE Select ENSP00000342812.3:p.Ala1060Thr
ENST00000426564.6:n.3190G>A
NM_004654.3:c.3178G>A NP_004645.2:p.Ala1060Thr
XM_011531469.1:c.3178G>A XP_011529771.1:p.Ala1060Thr
XM_011531470.1:c.2944G>A XP_011529772.1:p.Ala982Thr
XM_017030078.2:c.3193G>A XP_016885567.1:p.Ala1065Thr
NM_004654.4:c.3178G>A MANE Select NP_004645.2:p.Ala1060Thr
Search 100 bp 5'
Search 100 bp 3'