Canonical Allele Identifier: CA2518351137

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12777950_12777951del , CM000686.2:g.12777950_12777951del	GRCh38
NC_000024.9:g.14889884_14889885del , CM000686.1:g.14889884_14889885del	GRCh37
NC_000024.8:g.13399278_13399279del	NCBI36
NG_008311.1:g.81725_81726del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-69_2640-68del	ENSP00000498372.1:n.2640-69_2640-68del
ENST00000338981.7:c.2640-69_2640-68del MANE Select	ENSP00000342812.3:n.2640-69_2640-68del
ENST00000426564.6:n.2652-69_2652-68del
NM_004654.3:c.2640-69_2640-68del	NP_004645.2:n.2640-69_2640-68del
XM_011531469.1:c.2640-69_2640-68del	XP_011529771.1:n.2640-69_2640-68del
XM_011531470.1:c.2406-69_2406-68del	XP_011529772.1:n.2406-69_2406-68del
XM_017030078.2:c.2655-69_2655-68del	XP_016885567.1:n.2655-69_2655-68del
NM_004654.4:c.2640-69_2640-68del MANE Select	NP_004645.2:n.2640-69_2640-68del