Canonical Allele Identifier: CA519893120

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890172A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778238A>G , CM000686.2:g.12778238A>G	GRCh38
NC_000024.9:g.14890172A>G , CM000686.1:g.14890172A>G	GRCh37
NC_000024.8:g.13399566A>G	NCBI36
NG_008311.1:g.82013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2859A>G	ENSP00000498372.1:p.Gln953=
ENST00000338981.7:c.2859A>G MANE Select	ENSP00000342812.3:p.Gln953=
ENST00000426564.6:n.2871A>G
NM_004654.3:c.2859A>G	NP_004645.2:p.Gln953=
XM_011531469.1:c.2859A>G	XP_011529771.1:p.Gln953=
XM_011531470.1:c.2625A>G	XP_011529772.1:p.Gln875=
XM_017030078.2:c.2874A>G	XP_016885567.1:p.Gln958=
NM_004654.4:c.2859A>G MANE Select	NP_004645.2:p.Gln953=