Canonical Allele Identifier: CA519891798
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14922723C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810788C>A , CM000686.2:g.12810788C>A GRCh38
NC_000024.9:g.14922723C>A , CM000686.1:g.14922723C>A GRCh37
NC_000024.8:g.13432117C>A NCBI36
NG_008311.1:g.114564C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4209C>A ENSP00000498372.1:p.Val1403=
ENST00000338981.7:c.4209C>A MANE Select ENSP00000342812.3:p.Val1403=
ENST00000426564.6:n.4221C>A
NM_004654.3:c.4209C>A NP_004645.2:p.Val1403=
XM_011531469.1:c.4209C>A XP_011529771.1:p.Val1403=
XM_011531470.1:c.3975C>A XP_011529772.1:p.Val1325=
XM_017030078.2:c.4224C>A XP_016885567.1:p.Val1408=
NM_004654.4:c.4209C>A MANE Select NP_004645.2:p.Val1403=