Canonical Allele Identifier: CA519865147

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14847590G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735656G>A , CM000686.2:g.12735656G>A	GRCh38
NC_000024.9:g.14847590G>A , CM000686.1:g.14847590G>A	GRCh37
NC_000024.8:g.13356984G>A	NCBI36
NG_008311.1:g.39431G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.702G>A	ENSP00000498372.1:p.Gly234=
ENST00000338981.7:c.702G>A MANE Select	ENSP00000342812.3:p.Gly234=
ENST00000426564.6:n.714G>A
NM_004654.3:c.702G>A	NP_004645.2:p.Gly234=
XM_011531469.1:c.702G>A	XP_011529771.1:p.Gly234=
XM_011531470.1:c.468G>A	XP_011529772.1:p.Gly156=
XM_017030078.2:c.702G>A	XP_016885567.1:p.Gly234=
NM_004654.4:c.702G>A MANE Select	NP_004645.2:p.Gly234=