Canonical Allele Identifier: CA2766242003
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833667_12833669del , CM000686.2:g.12833667_12833669del GRCh38
NC_000024.9:g.14945593_14945595del , CM000686.1:g.14945593_14945595del GRCh37
NC_000024.8:g.13454987_13454989del NCBI36
NG_008311.1:g.137434_137436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5022-21_5022-19del ENSP00000498372.1:n.5022-21_5022-19del
ENST00000338981.7:c.5022-21_5022-19del MANE Select ENSP00000342812.3:n.5022-21_5022-19del
ENST00000426564.6:n.5034-21_5034-19del
NM_004654.3:c.5022-21_5022-19del NP_004645.2:n.5022-21_5022-19del
XM_011531469.1:c.5022-21_5022-19del XP_011529771.1:n.5022-21_5022-19del
XM_011531470.1:c.4788-21_4788-19del XP_011529772.1:n.4788-21_4788-19del
XM_017030078.2:c.5037-21_5037-19del XP_016885567.1:n.5037-21_5037-19del
NM_004654.4:c.5022-21_5022-19del MANE Select NP_004645.2:n.5022-21_5022-19del