Canonical Allele Identifier: CA10573268
Gene: USP9Y HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790523A>G , CM000686.2:g.12790523A>G GRCh38
NC_000024.9:g.14902456A>G , CM000686.1:g.14902456A>G GRCh37
NC_000024.8:g.13411850A>G NCBI36
NG_008311.1:g.94297A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3678A>G ENSP00000498372.1:p.Ile1226Met
ENST00000338981.7:c.3678A>G MANE Select ENSP00000342812.3:p.Ile1226Met
ENST00000426564.6:n.3690A>G
NM_004654.3:c.3678A>G NP_004645.2:p.Ile1226Met
XM_011531469.1:c.3678A>G XP_011529771.1:p.Ile1226Met
XM_011531470.1:c.3444A>G XP_011529772.1:p.Ile1148Met
XM_017030078.2:c.3693A>G XP_016885567.1:p.Ile1231Met
NM_004654.4:c.3678A>G MANE Select NP_004645.2:p.Ile1226Met