Canonical Allele Identifier: CA414989204
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810682G>A , CM000686.2:g.12810682G>A GRCh38
NC_000024.9:g.14922617G>A , CM000686.1:g.14922617G>A GRCh37
NC_000024.8:g.13432011G>A NCBI36
NG_008311.1:g.114458G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4103G>A ENSP00000498372.1:p.Arg1368Lys
ENST00000338981.7:c.4103G>A MANE Select ENSP00000342812.3:p.Arg1368Lys
ENST00000426564.6:n.4115G>A
NM_004654.3:c.4103G>A NP_004645.2:p.Arg1368Lys
XM_011531469.1:c.4103G>A XP_011529771.1:p.Arg1368Lys
XM_011531470.1:c.3869G>A XP_011529772.1:p.Arg1290Lys
XM_017030078.2:c.4118G>A XP_016885567.1:p.Arg1373Lys
NM_004654.4:c.4103G>A MANE Select NP_004645.2:p.Arg1368Lys