Canonical Allele Identifier: CA2470558100
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12789831_12789832delinsGT , CM000686.2:g.12789831_12789832delinsGT GRCh38
NC_000024.9:g.14901764_14901765delinsGT , CM000686.1:g.14901764_14901765delinsGT GRCh37
NC_000024.8:g.13411158_13411159delinsGT NCBI36
NG_008311.1:g.93605_93606delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3562-576_3562-575delinsGT ENSP00000498372.1:n.3562-576_3562-575delinsGT
ENST00000338981.7:c.3562-576_3562-575delinsGT MANE Select ENSP00000342812.3:n.3562-576_3562-575delinsGT
ENST00000426564.6:n.3574-576_3574-575delinsGT
NM_004654.3:c.3562-576_3562-575delinsGT NP_004645.2:n.3562-576_3562-575delinsGT
XM_011531469.1:c.3562-576_3562-575delinsGT XP_011529771.1:n.3562-576_3562-575delinsGT
XM_011531470.1:c.3328-576_3328-575delinsGT XP_011529772.1:n.3328-576_3328-575delinsGT
XM_017030078.2:c.3577-576_3577-575delinsGT XP_016885567.1:n.3577-576_3577-575delinsGT
NM_004654.4:c.3562-576_3562-575delinsGT MANE Select NP_004645.2:n.3562-576_3562-575delinsGT