Canonical Allele Identifier: CA415007261

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14958258G>T (hg19) ; chrY:g.12846333G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846333G>T , CM000686.2:g.12846333G>T	GRCh38
NC_000024.9:g.14958258G>T , CM000686.1:g.14958258G>T	GRCh37
NC_000024.8:g.13467652G>T	NCBI36
NG_008311.1:g.150099G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.6569G>T	ENSP00000498372.1:p.Gly2190Val
ENST00000338981.7:c.6569G>T MANE Select	ENSP00000342812.3:p.Gly2190Val
ENST00000426564.6:n.6596G>T
NM_004654.3:c.6569G>T	NP_004645.2:p.Gly2190Val
XM_011531469.1:c.6569G>T	XP_011529771.1:p.Gly2190Val
XM_011531470.1:c.6335G>T	XP_011529772.1:p.Gly2112Val
XM_017030078.2:c.6584G>T	XP_016885567.1:p.Gly2195Val
NM_004654.4:c.6569G>T MANE Select	NP_004645.2:p.Gly2190Val