Canonical Allele Identifier: CA414980708
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720689C>G , CM000686.2:g.12720689C>G GRCh38
NC_000024.9:g.14832622C>G , CM000686.1:g.14832622C>G GRCh37
NC_000024.8:g.13342016C>G NCBI36
NG_008311.1:g.24463C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.197C>G ENSP00000498372.1:p.Pro66Arg
ENST00000338981.7:c.197C>G MANE Select ENSP00000342812.3:p.Pro66Arg
ENST00000426564.6:n.209C>G
ENST00000493168.1:n.273C>G
NM_004654.3:c.197C>G NP_004645.2:p.Pro66Arg
XM_011531469.1:c.197C>G XP_011529771.1:p.Pro66Arg
XM_011531470.1:c.-38C>G XP_011529772.1:n.-38C>G
XM_017030078.2:c.197C>G XP_016885567.1:p.Pro66Arg
NM_004654.4:c.197C>G MANE Select NP_004645.2:p.Pro66Arg