Canonical Allele Identifier: CA10573193
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs34601266
gnomAD v2: Y-14889974-C-T
gnomAD v3: Y-12778040-C-T
gnomAD v4: Y-12778040-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778040C>T , CM000686.2:g.12778040C>T GRCh38
NC_000024.9:g.14889974C>T , CM000686.1:g.14889974C>T GRCh37
NC_000024.8:g.13399368C>T NCBI36
NG_008311.1:g.81815C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2661C>T ENSP00000498372.1:p.Leu887=
ENST00000338981.7:c.2661C>T MANE Select ENSP00000342812.3:p.Leu887=
ENST00000426564.6:n.2673C>T
NM_004654.3:c.2661C>T NP_004645.2:p.Leu887=
XM_011531469.1:c.2661C>T XP_011529771.1:p.Leu887=
XM_011531470.1:c.2427C>T XP_011529772.1:p.Leu809=
XM_017030078.2:c.2676C>T XP_016885567.1:p.Leu892=
NM_004654.4:c.2661C>T MANE Select NP_004645.2:p.Leu887=