Canonical Allele Identifier: CA2766240792
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735928A>G , CM000686.2:g.12735928A>G GRCh38
NC_000024.9:g.14847862A>G , CM000686.1:g.14847862A>G GRCh37
NC_000024.8:g.13357256A>G NCBI36
NG_008311.1:g.39703A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.774-70A>G ENSP00000498372.1:n.774-70A>G
ENST00000338981.7:c.774-70A>G MANE Select ENSP00000342812.3:n.774-70A>G
ENST00000426564.6:n.786-70A>G
NM_004654.3:c.774-70A>G NP_004645.2:n.774-70A>G
XM_011531469.1:c.774-70A>G XP_011529771.1:n.774-70A>G
XM_011531470.1:c.540-70A>G XP_011529772.1:n.540-70A>G
XM_017030078.2:c.774-70A>G XP_016885567.1:n.774-70A>G
NM_004654.4:c.774-70A>G MANE Select NP_004645.2:n.774-70A>G