Canonical Allele Identifier: CA2579748038
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833620T>C , CM000686.2:g.12833620T>C GRCh38
NC_000024.9:g.14945546T>C , CM000686.1:g.14945546T>C GRCh37
NC_000024.8:g.13454940T>C NCBI36
NG_008311.1:g.137387T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.5022-68T>C ENSP00000498372.1:n.5022-68T>C
ENST00000338981.7:c.5022-68T>C MANE Select ENSP00000342812.3:n.5022-68T>C
ENST00000426564.6:n.5034-68T>C
NM_004654.3:c.5022-68T>C NP_004645.2:n.5022-68T>C
XM_011531469.1:c.5022-68T>C XP_011529771.1:n.5022-68T>C
XM_011531470.1:c.4788-68T>C XP_011529772.1:n.4788-68T>C
XM_017030078.2:c.5037-68T>C XP_016885567.1:n.5037-68T>C
NM_004654.4:c.5022-68T>C MANE Select NP_004645.2:n.5022-68T>C
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