Canonical Allele Identifier: CA414992692
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14924940T>C (hg19) chrY:g.12813005T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12813005T>C , CM000686.2:g.12813005T>C GRCh38
NC_000024.9:g.14924940T>C , CM000686.1:g.14924940T>C GRCh37
NC_000024.8:g.13434334T>C NCBI36
NG_008311.1:g.116781T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4562T>C ENSP00000498372.1:p.Ile1521Thr
ENST00000338981.7:c.4562T>C MANE Select ENSP00000342812.3:p.Ile1521Thr
ENST00000426564.6:n.4574T>C
NM_004654.3:c.4562T>C NP_004645.2:p.Ile1521Thr
XM_011531469.1:c.4562T>C XP_011529771.1:p.Ile1521Thr
XM_011531470.1:c.4328T>C XP_011529772.1:p.Ile1443Thr
XM_017030078.2:c.4577T>C XP_016885567.1:p.Ile1526Thr
NM_004654.4:c.4562T>C MANE Select NP_004645.2:p.Ile1521Thr
Search 100 bp 5'
Search 100 bp 3'