Canonical Allele Identifier: CA2766241941
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12818321C>T , CM000686.2:g.12818321C>T GRCh38
NC_000024.9:g.14930256C>T , CM000686.1:g.14930256C>T GRCh37
NC_000024.8:g.13439650C>T NCBI36
NG_008311.1:g.122097C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4831-99C>T ENSP00000498372.1:n.4831-99C>T
ENST00000338981.7:c.4831-99C>T MANE Select ENSP00000342812.3:n.4831-99C>T
ENST00000426564.6:n.4843-99C>T
NM_004654.3:c.4831-99C>T NP_004645.2:n.4831-99C>T
XM_011531469.1:c.4831-99C>T XP_011529771.1:n.4831-99C>T
XM_011531470.1:c.4597-99C>T XP_011529772.1:n.4597-99C>T
XM_017030078.2:c.4846-99C>T XP_016885567.1:n.4846-99C>T
NM_004654.4:c.4831-99C>T MANE Select NP_004645.2:n.4831-99C>T