Canonical Allele Identifier: CA519857102
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053435065
MyVariant Identifiers: chrY:g.14832626A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720693A>G , CM000686.2:g.12720693A>G GRCh38
NC_000024.9:g.14832626A>G , CM000686.1:g.14832626A>G GRCh37
NC_000024.8:g.13342020A>G NCBI36
NG_008311.1:g.24467A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.201A>G ENSP00000498372.1:p.Ala67=
ENST00000338981.7:c.201A>G MANE Select ENSP00000342812.3:p.Ala67=
ENST00000426564.6:n.213A>G
ENST00000493168.1:n.277A>G
NM_004654.3:c.201A>G NP_004645.2:p.Ala67=
XM_011531469.1:c.201A>G XP_011529771.1:p.Ala67=
XM_011531470.1:c.-34A>G XP_011529772.1:n.-34A>G
XM_017030078.2:c.201A>G XP_016885567.1:p.Ala67=
NM_004654.4:c.201A>G MANE Select NP_004645.2:p.Ala67=