Canonical Allele Identifier: CA2470560437
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833580G= , CM000686.2:g.12833580G= GRCh38
NC_000024.9:g.14945506G= , CM000686.1:g.14945506G= GRCh37
NC_000024.8:g.13454900G= NCBI36
NG_008311.1:g.137347G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5022-108G= ENSP00000498372.1:n.5022-108G=
ENST00000338981.7:c.5022-108G= MANE Select ENSP00000342812.3:n.5022-108G=
ENST00000426564.6:n.5034-108G=
NM_004654.3:c.5022-108G= NP_004645.2:n.5022-108G=
XM_011531469.1:c.5022-108G= XP_011529771.1:n.5022-108G=
XM_011531470.1:c.4788-108G= XP_011529772.1:n.4788-108G=
XM_017030078.2:c.5037-108G= XP_016885567.1:n.5037-108G=
NM_004654.4:c.5022-108G= MANE Select NP_004645.2:n.5022-108G=