Canonical Allele Identifier: CA414989191
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810679C>G , CM000686.2:g.12810679C>G GRCh38
NC_000024.9:g.14922614C>G , CM000686.1:g.14922614C>G GRCh37
NC_000024.8:g.13432008C>G NCBI36
NG_008311.1:g.114455C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4100C>G ENSP00000498372.1:p.Ala1367Gly
ENST00000338981.7:c.4100C>G MANE Select ENSP00000342812.3:p.Ala1367Gly
ENST00000426564.6:n.4112C>G
NM_004654.3:c.4100C>G NP_004645.2:p.Ala1367Gly
XM_011531469.1:c.4100C>G XP_011529771.1:p.Ala1367Gly
XM_011531470.1:c.3866C>G XP_011529772.1:p.Ala1289Gly
XM_017030078.2:c.4115C>G XP_016885567.1:p.Ala1372Gly
NM_004654.4:c.4100C>G MANE Select NP_004645.2:p.Ala1367Gly