Canonical Allele Identifier: CA415008070
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778104A>C , CM000686.2:g.12778104A>C GRCh38
NC_000024.9:g.14890038A>C , CM000686.1:g.14890038A>C GRCh37
NC_000024.8:g.13399432A>C NCBI36
NG_008311.1:g.81879A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2725A>C ENSP00000498372.1:p.Thr909Pro
ENST00000338981.7:c.2725A>C MANE Select ENSP00000342812.3:p.Thr909Pro
ENST00000426564.6:n.2737A>C
NM_004654.3:c.2725A>C NP_004645.2:p.Thr909Pro
XM_011531469.1:c.2725A>C XP_011529771.1:p.Thr909Pro
XM_011531470.1:c.2491A>C XP_011529772.1:p.Thr831Pro
XM_017030078.2:c.2740A>C XP_016885567.1:p.Thr914Pro
NM_004654.4:c.2725A>C MANE Select NP_004645.2:p.Thr909Pro