Canonical Allele Identifier: CA1139769288

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12777986_12777988delinsTTT , CM000686.2:g.12777986_12777988delinsTTT	GRCh38
NC_000024.9:g.14889920_14889922delinsTTT , CM000686.1:g.14889920_14889922delinsTTT	GRCh37
NC_000024.8:g.13399314_13399316delinsTTT	NCBI36
NG_008311.1:g.81761_81763delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-33_2640-31delinsTTT	ENSP00000498372.1:n.2640-33_2640-31delinsTTT
ENST00000338981.7:c.2640-33_2640-31delinsTTT MANE Select	ENSP00000342812.3:n.2640-33_2640-31delinsTTT
ENST00000426564.6:n.2652-33_2652-31delinsTTT
NM_004654.3:c.2640-33_2640-31delinsTTT	NP_004645.2:n.2640-33_2640-31delinsTTT
XM_011531469.1:c.2640-33_2640-31delinsTTT	XP_011529771.1:n.2640-33_2640-31delinsTTT
XM_011531470.1:c.2406-33_2406-31delinsTTT	XP_011529772.1:n.2406-33_2406-31delinsTTT
XM_017030078.2:c.2655-33_2655-31delinsTTT	XP_016885567.1:n.2655-33_2655-31delinsTTT
NM_004654.4:c.2640-33_2640-31delinsTTT MANE Select	NP_004645.2:n.2640-33_2640-31delinsTTT