Canonical Allele Identifier: CA414983623
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12790447-G-T
gnomAD v4: Y-12790447-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790447G>T , CM000686.2:g.12790447G>T GRCh38
NC_000024.9:g.14902380G>T , CM000686.1:g.14902380G>T GRCh37
NC_000024.8:g.13411774G>T NCBI36
NG_008311.1:g.94221G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3602G>T ENSP00000498372.1:p.Ser1201Ile
ENST00000338981.7:c.3602G>T MANE Select ENSP00000342812.3:p.Ser1201Ile
ENST00000426564.6:n.3614G>T
NM_004654.3:c.3602G>T NP_004645.2:p.Ser1201Ile
XM_011531469.1:c.3602G>T XP_011529771.1:p.Ser1201Ile
XM_011531470.1:c.3368G>T XP_011529772.1:p.Ser1123Ile
XM_017030078.2:c.3617G>T XP_016885567.1:p.Ser1206Ile
NM_004654.4:c.3602G>T MANE Select NP_004645.2:p.Ser1201Ile