Canonical Allele Identifier: CA414998973

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14945695A>C (hg19) ; chrY:g.12833769A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833769A>C , CM000686.2:g.12833769A>C	GRCh38
NC_000024.9:g.14945695A>C , CM000686.1:g.14945695A>C	GRCh37
NC_000024.8:g.13455089A>C	NCBI36
NG_008311.1:g.137536A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5103A>C	ENSP00000498372.1:p.Glu1701Asp
ENST00000338981.7:c.5103A>C MANE Select	ENSP00000342812.3:p.Glu1701Asp
ENST00000426564.6:n.5115A>C
NM_004654.3:c.5103A>C	NP_004645.2:p.Glu1701Asp
XM_011531469.1:c.5103A>C	XP_011529771.1:p.Glu1701Asp
XM_011531470.1:c.4869A>C	XP_011529772.1:p.Glu1623Asp
XM_017030078.2:c.5118A>C	XP_016885567.1:p.Glu1706Asp
NM_004654.4:c.5103A>C MANE Select	NP_004645.2:p.Glu1701Asp