Canonical Allele Identifier: CA2556910828

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12777942_12777943insAA , CM000686.2:g.12777942_12777943insAA	GRCh38
NC_000024.9:g.14889876_14889877insAA , CM000686.1:g.14889876_14889877insAA	GRCh37
NC_000024.8:g.13399270_13399271insAA	NCBI36
NG_008311.1:g.81717_81718insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-77_2640-76insAA	ENSP00000498372.1:n.2640-77_2640-76insAA
ENST00000338981.7:c.2640-77_2640-76insAA MANE Select	ENSP00000342812.3:n.2640-77_2640-76insAA
ENST00000426564.6:n.2652-77_2652-76insAA
NM_004654.3:c.2640-77_2640-76insAA	NP_004645.2:n.2640-77_2640-76insAA
XM_011531469.1:c.2640-77_2640-76insAA	XP_011529771.1:n.2640-77_2640-76insAA
XM_011531470.1:c.2406-77_2406-76insAA	XP_011529772.1:n.2406-77_2406-76insAA
XM_017030078.2:c.2655-77_2655-76insAA	XP_016885567.1:n.2655-77_2655-76insAA
NM_004654.4:c.2640-77_2640-76insAA MANE Select	NP_004645.2:n.2640-77_2640-76insAA