Canonical Allele Identifier: CA415008298

Gene: USP9Y

Linked Data

• COSMIC: COSM4167361
• MyVariant Identifiers: chrY:g.14890066G>T (hg19) ; chrY:g.12778132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778132G>T , CM000686.2:g.12778132G>T	GRCh38
NC_000024.9:g.14890066G>T , CM000686.1:g.14890066G>T	GRCh37
NC_000024.8:g.13399460G>T	NCBI36
NG_008311.1:g.81907G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2753G>T	ENSP00000498372.1:p.Arg918Leu
ENST00000338981.7:c.2753G>T MANE Select	ENSP00000342812.3:p.Arg918Leu
ENST00000426564.6:n.2765G>T
NM_004654.3:c.2753G>T	NP_004645.2:p.Arg918Leu
XM_011531469.1:c.2753G>T	XP_011529771.1:p.Arg918Leu
XM_011531470.1:c.2519G>T	XP_011529772.1:p.Arg840Leu
XM_017030078.2:c.2768G>T	XP_016885567.1:p.Arg923Leu
NM_004654.4:c.2753G>T MANE Select	NP_004645.2:p.Arg918Leu