Canonical Allele Identifier: CA414992034

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14924841A>C (hg19) ; chrY:g.12812906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12812906A>C , CM000686.2:g.12812906A>C	GRCh38
NC_000024.9:g.14924841A>C , CM000686.1:g.14924841A>C	GRCh37
NC_000024.8:g.13434235A>C	NCBI36
NG_008311.1:g.116682A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.4463A>C	ENSP00000498372.1:p.Glu1488Ala
ENST00000338981.7:c.4463A>C MANE Select	ENSP00000342812.3:p.Glu1488Ala
ENST00000426564.6:n.4475A>C
NM_004654.3:c.4463A>C	NP_004645.2:p.Glu1488Ala
XM_011531469.1:c.4463A>C	XP_011529771.1:p.Glu1488Ala
XM_011531470.1:c.4229A>C	XP_011529772.1:p.Glu1410Ala
XM_017030078.2:c.4478A>C	XP_016885567.1:p.Glu1493Ala
NM_004654.4:c.4463A>C MANE Select	NP_004645.2:p.Glu1488Ala