Canonical Allele Identifier: CA10573580

Gene: USP9Y

Linked Data

• dbSNP Id: rs764850625
• ExAC: Y:14969567 C / A
• gnomAD v2: Y-14969567-C-A
• MyVariant Identifiers: chrY:g.14969567C>A (hg19) ; chrY:g.12857642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857642C>A , CM000686.2:g.12857642C>A	GRCh38
NC_000024.9:g.14969567C>A , CM000686.1:g.14969567C>A	GRCh37
NC_000024.8:g.13478961C>A	NCBI36
NG_008311.1:g.161408C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7511C>A	ENSP00000498372.1:p.Pro2504His
ENST00000338981.7:c.7511C>A MANE Select	ENSP00000342812.3:p.Pro2504His
ENST00000426564.6:n.7538C>A
ENST00000453031.1:c.556C>A
ENST00000471409.1:n.830C>A
NM_004654.3:c.7511C>A	NP_004645.2:p.Pro2504His
XM_011531469.1:c.7511C>A	XP_011529771.1:p.Pro2504His
XM_011531470.1:c.7277C>A	XP_011529772.1:p.Pro2426His
XM_017030078.2:c.7526C>A	XP_016885567.1:p.Pro2509His
NM_004654.4:c.7511C>A MANE Select	NP_004645.2:p.Pro2504His