Canonical Allele Identifier: CA414983364
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790407A>T , CM000686.2:g.12790407A>T GRCh38
NC_000024.9:g.14902340A>T , CM000686.1:g.14902340A>T GRCh37
NC_000024.8:g.13411734A>T NCBI36
NG_008311.1:g.94181A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3562A>T ENSP00000498372.1:p.Ile1188Phe
ENST00000338981.7:c.3562A>T MANE Select ENSP00000342812.3:p.Ile1188Phe
ENST00000426564.6:n.3574A>T
NM_004654.3:c.3562A>T NP_004645.2:p.Ile1188Phe
XM_011531469.1:c.3562A>T XP_011529771.1:p.Ile1188Phe
XM_011531470.1:c.3328A>T XP_011529772.1:p.Ile1110Phe
XM_017030078.2:c.3577A>T XP_016885567.1:p.Ile1193Phe
NM_004654.4:c.3562A>T MANE Select NP_004645.2:p.Ile1188Phe