Canonical Allele Identifier: CA415007333
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12846348C>G , CM000686.2:g.12846348C>G GRCh38
NC_000024.9:g.14958273C>G , CM000686.1:g.14958273C>G GRCh37
NC_000024.8:g.13467667C>G NCBI36
NG_008311.1:g.150114C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.6584C>G ENSP00000498372.1:p.Thr2195Arg
ENST00000338981.7:c.6584C>G MANE Select ENSP00000342812.3:p.Thr2195Arg
ENST00000426564.6:n.6611C>G
NM_004654.3:c.6584C>G NP_004645.2:p.Thr2195Arg
XM_011531469.1:c.6584C>G XP_011529771.1:p.Thr2195Arg
XM_011531470.1:c.6350C>G XP_011529772.1:p.Thr2117Arg
XM_017030078.2:c.6599C>G XP_016885567.1:p.Thr2200Arg
NM_004654.4:c.6584C>G MANE Select NP_004645.2:p.Thr2195Arg