Canonical Allele Identifier: CA519892288

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890076T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778142T>A , CM000686.2:g.12778142T>A	GRCh38
NC_000024.9:g.14890076T>A , CM000686.1:g.14890076T>A	GRCh37
NC_000024.8:g.13399470T>A	NCBI36
NG_008311.1:g.81917T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2763T>A	ENSP00000498372.1:p.Val921=
ENST00000338981.7:c.2763T>A MANE Select	ENSP00000342812.3:p.Val921=
ENST00000426564.6:n.2775T>A
NM_004654.3:c.2763T>A	NP_004645.2:p.Val921=
XM_011531469.1:c.2763T>A	XP_011529771.1:p.Val921=
XM_011531470.1:c.2529T>A	XP_011529772.1:p.Val843=
XM_017030078.2:c.2778T>A	XP_016885567.1:p.Val926=
NM_004654.4:c.2763T>A MANE Select	NP_004645.2:p.Val921=