Canonical Allele Identifier: CA415008025

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890032T>G (hg19) ; chrY:g.12778098T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778098T>G , CM000686.2:g.12778098T>G	GRCh38
NC_000024.9:g.14890032T>G , CM000686.1:g.14890032T>G	GRCh37
NC_000024.8:g.13399426T>G	NCBI36
NG_008311.1:g.81873T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2719T>G	ENSP00000498372.1:p.Ser907Ala
ENST00000338981.7:c.2719T>G MANE Select	ENSP00000342812.3:p.Ser907Ala
ENST00000426564.6:n.2731T>G
NM_004654.3:c.2719T>G	NP_004645.2:p.Ser907Ala
XM_011531469.1:c.2719T>G	XP_011529771.1:p.Ser907Ala
XM_011531470.1:c.2485T>G	XP_011529772.1:p.Ser829Ala
XM_017030078.2:c.2734T>G	XP_016885567.1:p.Ser912Ala
NM_004654.4:c.2719T>G MANE Select	NP_004645.2:p.Ser907Ala