Canonical Allele Identifier: CA519901988
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14945758T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833832T>C , CM000686.2:g.12833832T>C GRCh38
NC_000024.9:g.14945758T>C , CM000686.1:g.14945758T>C GRCh37
NC_000024.8:g.13455152T>C NCBI36
NG_008311.1:g.137599T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5166T>C ENSP00000498372.1:p.Asp1722=
ENST00000338981.7:c.5166T>C MANE Select ENSP00000342812.3:p.Asp1722=
ENST00000426564.6:n.5178T>C
NM_004654.3:c.5166T>C NP_004645.2:p.Asp1722=
XM_011531469.1:c.5166T>C XP_011529771.1:p.Asp1722=
XM_011531470.1:c.4932T>C XP_011529772.1:p.Asp1644=
XM_017030078.2:c.5181T>C XP_016885567.1:p.Asp1727=
NM_004654.4:c.5166T>C MANE Select NP_004645.2:p.Asp1722=
Search 100 bp 5'
Search 100 bp 3'