Canonical Allele Identifier: CA414984219
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735649T>C , CM000686.2:g.12735649T>C GRCh38
NC_000024.9:g.14847583T>C , CM000686.1:g.14847583T>C GRCh37
NC_000024.8:g.13356977T>C NCBI36
NG_008311.1:g.39424T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.695T>C ENSP00000498372.1:p.Leu232Ser
ENST00000338981.7:c.695T>C MANE Select ENSP00000342812.3:p.Leu232Ser
ENST00000426564.6:n.707T>C
NM_004654.3:c.695T>C NP_004645.2:p.Leu232Ser
XM_011531469.1:c.695T>C XP_011529771.1:p.Leu232Ser
XM_011531470.1:c.461T>C XP_011529772.1:p.Leu154Ser
XM_017030078.2:c.695T>C XP_016885567.1:p.Leu232Ser
NM_004654.4:c.695T>C MANE Select NP_004645.2:p.Leu232Ser