Canonical Allele Identifier: CA519857080
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14832623T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720690T>A , CM000686.2:g.12720690T>A GRCh38
NC_000024.9:g.14832623T>A , CM000686.1:g.14832623T>A GRCh37
NC_000024.8:g.13342017T>A NCBI36
NG_008311.1:g.24464T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.198T>A ENSP00000498372.1:p.Pro66=
ENST00000338981.7:c.198T>A MANE Select ENSP00000342812.3:p.Pro66=
ENST00000426564.6:n.210T>A
ENST00000493168.1:n.274T>A
NM_004654.3:c.198T>A NP_004645.2:p.Pro66=
XM_011531469.1:c.198T>A XP_011529771.1:p.Pro66=
XM_011531470.1:c.-37T>A XP_011529772.1:n.-37T>A
XM_017030078.2:c.198T>A XP_016885567.1:p.Pro66=
NM_004654.4:c.198T>A MANE Select NP_004645.2:p.Pro66=