Canonical Allele Identifier: CA2824887233

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846273_12846274insATA , CM000686.2:g.12846273_12846274insATA	GRCh38
NC_000024.9:g.14958198_14958199insATA , CM000686.1:g.14958198_14958199insATA	GRCh37
NC_000024.8:g.13467592_13467593insATA	NCBI36
NG_008311.1:g.150039_150040insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.6569-60_6569-59insATA	ENSP00000498372.1:n.6569-60_6569-59insATA
ENST00000338981.7:c.6569-60_6569-59insATA MANE Select	ENSP00000342812.3:n.6569-60_6569-59insATA
ENST00000426564.6:n.6596-60_6596-59insATA
NM_004654.3:c.6569-60_6569-59insATA	NP_004645.2:n.6569-60_6569-59insATA
XM_011531469.1:c.6569-60_6569-59insATA	XP_011529771.1:n.6569-60_6569-59insATA
XM_011531470.1:c.6335-60_6335-59insATA	XP_011529772.1:n.6335-60_6335-59insATA
XM_017030078.2:c.6584-60_6584-59insATA	XP_016885567.1:n.6584-60_6584-59insATA
NM_004654.4:c.6569-60_6569-59insATA MANE Select	NP_004645.2:n.6569-60_6569-59insATA