Canonical Allele Identifier: CA1139170125

Gene: USP9Y

Linked Data

• dbSNP Id: rs2053451050
• gnomAD v3: Y-12735832-T-TC
• gnomAD v4: Y-12735832-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735832_12735833insC , CM000686.2:g.12735832_12735833insC	GRCh38
NC_000024.9:g.14847766_14847767insC , CM000686.1:g.14847766_14847767insC	GRCh37
NC_000024.8:g.13357160_13357161insC	NCBI36
NG_008311.1:g.39607_39608insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.773+105_773+106insC	ENSP00000498372.1:n.773+105_773+106insC
ENST00000338981.7:c.773+105_773+106insC MANE Select	ENSP00000342812.3:n.773+105_773+106insC
ENST00000426564.6:n.785+105_785+106insC
NM_004654.3:c.773+105_773+106insC	NP_004645.2:n.773+105_773+106insC
XM_011531469.1:c.773+105_773+106insC	XP_011529771.1:n.773+105_773+106insC
XM_011531470.1:c.539+39_539+40insC	XP_011529772.1:n.539+39_539+40insC
XM_017030078.2:c.773+105_773+106insC	XP_016885567.1:n.773+105_773+106insC
NM_004654.4:c.773+105_773+106insC MANE Select	NP_004645.2:n.773+105_773+106insC