Canonical Allele Identifier: CA414984296

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14847593C>A (hg19) ; chrY:g.12735659C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735659C>A , CM000686.2:g.12735659C>A	GRCh38
NC_000024.9:g.14847593C>A , CM000686.1:g.14847593C>A	GRCh37
NC_000024.8:g.13356987C>A	NCBI36
NG_008311.1:g.39434C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.705C>A	ENSP00000498372.1:p.Phe235Leu
ENST00000338981.7:c.705C>A MANE Select	ENSP00000342812.3:p.Phe235Leu
ENST00000426564.6:n.717C>A
NM_004654.3:c.705C>A	NP_004645.2:p.Phe235Leu
XM_011531469.1:c.705C>A	XP_011529771.1:p.Phe235Leu
XM_011531470.1:c.471C>A	XP_011529772.1:p.Phe157Leu
XM_017030078.2:c.705C>A	XP_016885567.1:p.Phe235Leu
NM_004654.4:c.705C>A MANE Select	NP_004645.2:p.Phe235Leu