Canonical Allele Identifier: CA2766241279
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777939T>G , CM000686.2:g.12777939T>G GRCh38
NC_000024.9:g.14889873T>G , CM000686.1:g.14889873T>G GRCh37
NC_000024.8:g.13399267T>G NCBI36
NG_008311.1:g.81714T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2640-80T>G ENSP00000498372.1:n.2640-80T>G
ENST00000338981.7:c.2640-80T>G MANE Select ENSP00000342812.3:n.2640-80T>G
ENST00000426564.6:n.2652-80T>G
NM_004654.3:c.2640-80T>G NP_004645.2:n.2640-80T>G
XM_011531469.1:c.2640-80T>G XP_011529771.1:n.2640-80T>G
XM_011531470.1:c.2406-80T>G XP_011529772.1:n.2406-80T>G
XM_017030078.2:c.2655-80T>G XP_016885567.1:n.2655-80T>G
NM_004654.4:c.2640-80T>G MANE Select NP_004645.2:n.2640-80T>G