Canonical Allele Identifier: CA519901847
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14945725A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833799A>C , CM000686.2:g.12833799A>C GRCh38
NC_000024.9:g.14945725A>C , CM000686.1:g.14945725A>C GRCh37
NC_000024.8:g.13455119A>C NCBI36
NG_008311.1:g.137566A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5133A>C ENSP00000498372.1:p.Ile1711=
ENST00000338981.7:c.5133A>C MANE Select ENSP00000342812.3:p.Ile1711=
ENST00000426564.6:n.5145A>C
NM_004654.3:c.5133A>C NP_004645.2:p.Ile1711=
XM_011531469.1:c.5133A>C XP_011529771.1:p.Ile1711=
XM_011531470.1:c.4899A>C XP_011529772.1:p.Ile1633=
XM_017030078.2:c.5148A>C XP_016885567.1:p.Ile1716=
NM_004654.4:c.5133A>C MANE Select NP_004645.2:p.Ile1711=
Search 100 bp 5'
Search 100 bp 3'