Canonical Allele Identifier: CA519860637

Gene: USP9Y

Linked Data

• gnomAD v3: Y-12790532-G-A
• gnomAD v4: Y-12790532-G-A
• MyVariant Identifiers: chrY:g.14902465G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12790532G>A , CM000686.2:g.12790532G>A	GRCh38
NC_000024.9:g.14902465G>A , CM000686.1:g.14902465G>A	GRCh37
NC_000024.8:g.13411859G>A	NCBI36
NG_008311.1:g.94306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.3687G>A	ENSP00000498372.1:p.Glu1229=
ENST00000338981.7:c.3687G>A MANE Select	ENSP00000342812.3:p.Glu1229=
ENST00000426564.6:n.3699G>A
NM_004654.3:c.3687G>A	NP_004645.2:p.Glu1229=
XM_011531469.1:c.3687G>A	XP_011529771.1:p.Glu1229=
XM_011531470.1:c.3453G>A	XP_011529772.1:p.Glu1151=
XM_017030078.2:c.3702G>A	XP_016885567.1:p.Glu1234=
NM_004654.4:c.3687G>A MANE Select	NP_004645.2:p.Glu1229=