Canonical Allele Identifier: CA414999264
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833851T>C , CM000686.2:g.12833851T>C GRCh38
NC_000024.9:g.14945777T>C , CM000686.1:g.14945777T>C GRCh37
NC_000024.8:g.13455171T>C NCBI36
NG_008311.1:g.137618T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5185T>C ENSP00000498372.1:p.Cys1729Arg
ENST00000338981.7:c.5185T>C MANE Select ENSP00000342812.3:p.Cys1729Arg
ENST00000426564.6:n.5197T>C
NM_004654.3:c.5185T>C NP_004645.2:p.Cys1729Arg
XM_011531469.1:c.5185T>C XP_011529771.1:p.Cys1729Arg
XM_011531470.1:c.4951T>C XP_011529772.1:p.Cys1651Arg
XM_017030078.2:c.5200T>C XP_016885567.1:p.Cys1734Arg
NM_004654.4:c.5185T>C MANE Select NP_004645.2:p.Cys1729Arg