Canonical Allele Identifier: CA414999079
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14945724T>G (hg19) chrY:g.12833798T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833798T>G , CM000686.2:g.12833798T>G GRCh38
NC_000024.9:g.14945724T>G , CM000686.1:g.14945724T>G GRCh37
NC_000024.8:g.13455118T>G NCBI36
NG_008311.1:g.137565T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5132T>G ENSP00000498372.1:p.Ile1711Arg
ENST00000338981.7:c.5132T>G MANE Select ENSP00000342812.3:p.Ile1711Arg
ENST00000426564.6:n.5144T>G
NM_004654.3:c.5132T>G NP_004645.2:p.Ile1711Arg
XM_011531469.1:c.5132T>G XP_011529771.1:p.Ile1711Arg
XM_011531470.1:c.4898T>G XP_011529772.1:p.Ile1633Arg
XM_017030078.2:c.5147T>G XP_016885567.1:p.Ile1716Arg
NM_004654.4:c.5132T>G MANE Select NP_004645.2:p.Ile1711Arg
Search 100 bp 5'
Search 100 bp 3'