Canonical Allele Identifier: CA10573060

Gene: USP9Y

Linked Data

• dbSNP Id: rs766104794
• ExAC: Y:14847610 G / A
• gnomAD v2: Y-14847610-G-A
• MyVariant Identifiers: chrY:g.14847610G>A (hg19) ; chrY:g.12735676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735676G>A , CM000686.2:g.12735676G>A	GRCh38
NC_000024.9:g.14847610G>A , CM000686.1:g.14847610G>A	GRCh37
NC_000024.8:g.13357004G>A	NCBI36
NG_008311.1:g.39451G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.722G>A	ENSP00000498372.1:p.Arg241His
ENST00000338981.7:c.722G>A MANE Select	ENSP00000342812.3:p.Arg241His
ENST00000426564.6:n.734G>A
NM_004654.3:c.722G>A	NP_004645.2:p.Arg241His
XM_011531469.1:c.722G>A	XP_011529771.1:p.Arg241His
XM_011531470.1:c.488G>A	XP_011529772.1:p.Arg163His
XM_017030078.2:c.722G>A	XP_016885567.1:p.Arg241His
NM_004654.4:c.722G>A MANE Select	NP_004645.2:p.Arg241His