Canonical Allele Identifier: CA2766242011
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833889T>C , CM000686.2:g.12833889T>C GRCh38
NC_000024.9:g.14945815T>C , CM000686.1:g.14945815T>C GRCh37
NC_000024.8:g.13455209T>C NCBI36
NG_008311.1:g.137656T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5195+28T>C ENSP00000498372.1:n.5195+28T>C
ENST00000338981.7:c.5195+28T>C MANE Select ENSP00000342812.3:n.5195+28T>C
ENST00000426564.6:n.5207+28T>C
NM_004654.3:c.5195+28T>C NP_004645.2:n.5195+28T>C
XM_011531469.1:c.5195+28T>C XP_011529771.1:n.5195+28T>C
XM_011531470.1:c.4961+28T>C XP_011529772.1:n.4961+28T>C
XM_017030078.2:c.5210+28T>C XP_016885567.1:n.5210+28T>C
NM_004654.4:c.5195+28T>C MANE Select NP_004645.2:n.5195+28T>C