Canonical Allele Identifier: CA2470561816
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857643T= , CM000686.2:g.12857643T= GRCh38
NC_000024.9:g.14969568T= , CM000686.1:g.14969568T= GRCh37
NC_000024.8:g.13478962T= NCBI36
NG_008311.1:g.161409T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7512T= ENSP00000498372.1:p.Pro2504=
ENST00000338981.7:c.7512T= MANE Select ENSP00000342812.3:p.Pro2504=
ENST00000426564.6:n.7539T=
ENST00000453031.1:c.557T=
ENST00000471409.1:n.831T=
NM_004654.3:c.7512T= NP_004645.2:p.Pro2504=
XM_011531469.1:c.7512T= XP_011529771.1:p.Pro2504=
XM_011531470.1:c.7278T= XP_011529772.1:p.Pro2426=
XM_017030078.2:c.7527T= XP_016885567.1:p.Pro2509=
NM_004654.4:c.7512T= MANE Select NP_004645.2:p.Pro2504=