Canonical Allele Identifier: CA414998832

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14945665T>G (hg19) ; chrY:g.12833739T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833739T>G , CM000686.2:g.12833739T>G	GRCh38
NC_000024.9:g.14945665T>G , CM000686.1:g.14945665T>G	GRCh37
NC_000024.8:g.13455059T>G	NCBI36
NG_008311.1:g.137506T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5073T>G	ENSP00000498372.1:p.Phe1691Leu
ENST00000338981.7:c.5073T>G MANE Select	ENSP00000342812.3:p.Phe1691Leu
ENST00000426564.6:n.5085T>G
NM_004654.3:c.5073T>G	NP_004645.2:p.Phe1691Leu
XM_011531469.1:c.5073T>G	XP_011529771.1:p.Phe1691Leu
XM_011531470.1:c.4839T>G	XP_011529772.1:p.Phe1613Leu
XM_017030078.2:c.5088T>G	XP_016885567.1:p.Phe1696Leu
NM_004654.4:c.5073T>G MANE Select	NP_004645.2:p.Phe1691Leu