Canonical Allele Identifier: CA2470559323
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12812691T= , CM000686.2:g.12812691T= GRCh38
NC_000024.9:g.14924626T= , CM000686.1:g.14924626T= GRCh37
NC_000024.8:g.13434020T= NCBI36
NG_008311.1:g.116467T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4387-139T= ENSP00000498372.1:n.4387-139T=
ENST00000338981.7:c.4387-139T= MANE Select ENSP00000342812.3:n.4387-139T=
ENST00000426564.6:n.4399-139T=
NM_004654.3:c.4387-139T= NP_004645.2:n.4387-139T=
XM_011531469.1:c.4387-139T= XP_011529771.1:n.4387-139T=
XM_011531470.1:c.4153-139T= XP_011529772.1:n.4153-139T=
XM_017030078.2:c.4402-139T= XP_016885567.1:n.4402-139T=
NM_004654.4:c.4387-139T= MANE Select NP_004645.2:n.4387-139T=