Canonical Allele Identifier: CA519901884

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14945734A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833808A>G , CM000686.2:g.12833808A>G	GRCh38
NC_000024.9:g.14945734A>G , CM000686.1:g.14945734A>G	GRCh37
NC_000024.8:g.13455128A>G	NCBI36
NG_008311.1:g.137575A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5142A>G	ENSP00000498372.1:p.Lys1714=
ENST00000338981.7:c.5142A>G MANE Select	ENSP00000342812.3:p.Lys1714=
ENST00000426564.6:n.5154A>G
NM_004654.3:c.5142A>G	NP_004645.2:p.Lys1714=
XM_011531469.1:c.5142A>G	XP_011529771.1:p.Lys1714=
XM_011531470.1:c.4908A>G	XP_011529772.1:p.Lys1636=
XM_017030078.2:c.5157A>G	XP_016885567.1:p.Lys1719=
NM_004654.4:c.5142A>G MANE Select	NP_004645.2:p.Lys1714=