Canonical Allele Identifier: CA519890823
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1355447010
gnomAD v2: Y-14922624-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810689G>A , CM000686.2:g.12810689G>A GRCh38
NC_000024.9:g.14922624G>A , CM000686.1:g.14922624G>A GRCh37
NC_000024.8:g.13432018G>A NCBI36
NG_008311.1:g.114465G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4110G>A ENSP00000498372.1:p.Lys1370=
ENST00000338981.7:c.4110G>A MANE Select ENSP00000342812.3:p.Lys1370=
ENST00000426564.6:n.4122G>A
NM_004654.3:c.4110G>A NP_004645.2:p.Lys1370=
XM_011531469.1:c.4110G>A XP_011529771.1:p.Lys1370=
XM_011531470.1:c.3876G>A XP_011529772.1:p.Lys1292=
XM_017030078.2:c.4125G>A XP_016885567.1:p.Lys1375=
NM_004654.4:c.4110G>A MANE Select NP_004645.2:p.Lys1370=