Canonical Allele Identifier: CA414990038

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14922710A>T (hg19) ; chrY:g.12810775A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12810775A>T , CM000686.2:g.12810775A>T	GRCh38
NC_000024.9:g.14922710A>T , CM000686.1:g.14922710A>T	GRCh37
NC_000024.8:g.13432104A>T	NCBI36
NG_008311.1:g.114551A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.4196A>T	ENSP00000498372.1:p.Glu1399Val
ENST00000338981.7:c.4196A>T MANE Select	ENSP00000342812.3:p.Glu1399Val
ENST00000426564.6:n.4208A>T
NM_004654.3:c.4196A>T	NP_004645.2:p.Glu1399Val
XM_011531469.1:c.4196A>T	XP_011529771.1:p.Glu1399Val
XM_011531470.1:c.3962A>T	XP_011529772.1:p.Glu1321Val
XM_017030078.2:c.4211A>T	XP_016885567.1:p.Glu1404Val
NM_004654.4:c.4196A>T MANE Select	NP_004645.2:p.Glu1399Val