Canonical Allele Identifier: CA2824886456
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12812695_12812698del , CM000686.2:g.12812695_12812698del GRCh38
NC_000024.9:g.14924630_14924633del , CM000686.1:g.14924630_14924633del GRCh37
NC_000024.8:g.13434024_13434027del NCBI36
NG_008311.1:g.116471_116474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4387-135_4387-132del ENSP00000498372.1:n.4387-135_4387-132del
ENST00000338981.7:c.4387-135_4387-132del MANE Select ENSP00000342812.3:n.4387-135_4387-132del
ENST00000426564.6:n.4399-135_4399-132del
NM_004654.3:c.4387-135_4387-132del NP_004645.2:n.4387-135_4387-132del
XM_011531469.1:c.4387-135_4387-132del XP_011529771.1:n.4387-135_4387-132del
XM_011531470.1:c.4153-135_4153-132del XP_011529772.1:n.4153-135_4153-132del
XM_017030078.2:c.4402-135_4402-132del XP_016885567.1:n.4402-135_4402-132del
NM_004654.4:c.4387-135_4387-132del MANE Select NP_004645.2:n.4387-135_4387-132del