Canonical Allele Identifier: CA414986785
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857661G>C , CM000686.2:g.12857661G>C GRCh38
NC_000024.9:g.14969586G>C , CM000686.1:g.14969586G>C GRCh37
NC_000024.8:g.13478980G>C NCBI36
NG_008311.1:g.161427G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7530G>C ENSP00000498372.1:p.Gln2510His
ENST00000338981.7:c.7530G>C MANE Select ENSP00000342812.3:p.Gln2510His
ENST00000426564.6:n.7557G>C
ENST00000453031.1:c.575G>C
ENST00000471409.1:n.849G>C
NM_004654.3:c.7530G>C NP_004645.2:p.Gln2510His
XM_011531469.1:c.7530G>C XP_011529771.1:p.Gln2510His
XM_011531470.1:c.7296G>C XP_011529772.1:p.Gln2432His
XM_017030078.2:c.7545G>C XP_016885567.1:p.Gln2515His
NM_004654.4:c.7530G>C MANE Select NP_004645.2:p.Gln2510His