Canonical Allele Identifier: CA415009102

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890146G>T (hg19) ; chrY:g.12778212G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778212G>T , CM000686.2:g.12778212G>T	GRCh38
NC_000024.9:g.14890146G>T , CM000686.1:g.14890146G>T	GRCh37
NC_000024.8:g.13399540G>T	NCBI36
NG_008311.1:g.81987G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2833G>T	ENSP00000498372.1:p.Glu945Ter
ENST00000338981.7:c.2833G>T MANE Select	ENSP00000342812.3:p.Glu945Ter
ENST00000426564.6:n.2845G>T
NM_004654.3:c.2833G>T	NP_004645.2:p.Glu945Ter
XM_011531469.1:c.2833G>T	XP_011529771.1:p.Glu945Ter
XM_011531470.1:c.2599G>T	XP_011529772.1:p.Glu867Ter
XM_017030078.2:c.2848G>T	XP_016885567.1:p.Glu950Ter
NM_004654.4:c.2833G>T MANE Select	NP_004645.2:p.Glu945Ter