Canonical Allele Identifier: CA2766241276
Gene: USP9Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777933T>G , CM000686.2:g.12777933T>G GRCh38
NC_000024.9:g.14889867T>G , CM000686.1:g.14889867T>G GRCh37
NC_000024.8:g.13399261T>G NCBI36
NG_008311.1:g.81708T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2640-86T>G ENSP00000498372.1:n.2640-86T>G
ENST00000338981.7:c.2640-86T>G MANE Select ENSP00000342812.3:n.2640-86T>G
ENST00000426564.6:n.2652-86T>G
NM_004654.3:c.2640-86T>G NP_004645.2:n.2640-86T>G
XM_011531469.1:c.2640-86T>G XP_011529771.1:n.2640-86T>G
XM_011531470.1:c.2406-86T>G XP_011529772.1:n.2406-86T>G
XM_017030078.2:c.2655-86T>G XP_016885567.1:n.2655-86T>G
NM_004654.4:c.2640-86T>G MANE Select NP_004645.2:n.2640-86T>G
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