Canonical Allele Identifier: CA1139264734

Gene: USP9Y

Linked Data

• dbSNP Id: rs2053532822
• gnomAD v3: Y-12813009-A-AT
• gnomAD v4: Y-12813009-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12813009_12813010insT , CM000686.2:g.12813009_12813010insT	GRCh38
NC_000024.9:g.14924944_14924945insT , CM000686.1:g.14924944_14924945insT	GRCh37
NC_000024.8:g.13434338_13434339insT	NCBI36
NG_008311.1:g.116785_116786insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.4566_4567insT	ENSP00000498372.1:p.Asp1523Ter
ENST00000338981.7:c.4566_4567insT MANE Select	ENSP00000342812.3:p.Asp1523Ter
ENST00000426564.6:n.4578_4579insT
NM_004654.3:c.4566_4567insT	NP_004645.2:p.Asp1523Ter
XM_011531469.1:c.4566_4567insT	XP_011529771.1:p.Asp1523Ter
XM_011531470.1:c.4332_4333insT	XP_011529772.1:p.Asp1445Ter
XM_017030078.2:c.4581_4582insT	XP_016885567.1:p.Asp1528Ter
NM_004654.4:c.4566_4567insT MANE Select	NP_004645.2:p.Asp1523Ter