Canonical Allele Identifier: CA10573265
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs20321
gnomAD v2: Y-14902414-G-A
gnomAD v3: Y-12790481-G-A
gnomAD v4: Y-12790481-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790481G>A , CM000686.2:g.12790481G>A GRCh38
NC_000024.9:g.14902414G>A , CM000686.1:g.14902414G>A GRCh37
NC_000024.8:g.13411808G>A NCBI36
NG_008311.1:g.94255G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3636G>A ENSP00000498372.1:p.Glu1212=
ENST00000338981.7:c.3636G>A MANE Select ENSP00000342812.3:p.Glu1212=
ENST00000426564.6:n.3648G>A
NM_004654.3:c.3636G>A NP_004645.2:p.Glu1212=
XM_011531469.1:c.3636G>A XP_011529771.1:p.Glu1212=
XM_011531470.1:c.3402G>A XP_011529772.1:p.Glu1134=
XM_017030078.2:c.3651G>A XP_016885567.1:p.Glu1217=
NM_004654.4:c.3636G>A MANE Select NP_004645.2:p.Glu1212=