Canonical Allele Identifier: CA392398893

Gene: USP8

Linked Data

• gnomAD v4: 15-50490375-C-T
• MyVariant Identifiers: chr15:g.50782572C>T (hg19) ; chr15:g.50490375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490375C>T , CM000677.2:g.50490375C>T	GRCh38
NC_000015.9:g.50782572C>T , CM000677.1:g.50782572C>T	GRCh37
NC_000015.8:g.48569864C>T	NCBI36
NG_047101.1:g.70999C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2084C>T MANE Select	ENSP00000302239.4:p.Thr695Ile
ENST00000307179.8:c.2084C>T	ENSP00000302239.4:p.Thr695Ile
ENST00000396444.7:c.2084C>T	ENSP00000379721.3:p.Thr695Ile
ENST00000425032.7:c.1766C>T	ENSP00000412682.3:p.Thr589Ile
ENST00000561206.1:n.501C>T
NM_001128610.2:c.2084C>T	NP_001122082.1:p.Thr695Ile
NM_001283049.1:c.1766C>T	NP_001269978.1:p.Thr589Ile
NM_005154.4:c.2084C>T	NP_005145.3:p.Thr695Ile
XM_006720761.2:c.2084C>T	XP_006720824.1:p.Thr695Ile
XM_006720762.2:c.1997C>T	XP_006720825.1:p.Thr666Ile
XM_011522193.1:c.2084C>T	XP_011520495.1:p.Thr695Ile
XM_011522194.1:c.1412C>T	XP_011520496.1:p.Thr471Ile
XM_006720761.3:c.2084C>T	XP_006720824.1:p.Thr695Ile
XM_006720762.3:c.1997C>T	XP_006720825.1:p.Thr666Ile
XM_011522193.3:c.2084C>T	XP_011520495.1:p.Thr695Ile
XM_017022718.1:c.1997C>T	XP_016878207.1:p.Thr666Ile
XM_017022719.2:c.1997C>T	XP_016878208.1:p.Thr666Ile
XM_017022720.2:c.1997C>T	XP_016878209.1:p.Thr666Ile
XM_017022721.2:c.1514C>T	XP_016878210.1:p.Thr505Ile
XM_017022722.1:c.1514C>T	XP_016878211.1:p.Thr505Ile
XM_024450098.1:c.1514C>T	XP_024305866.1:p.Thr505Ile
NM_005154.5:c.2084C>T MANE Select	NP_005145.3:p.Thr695Ile
NM_001128610.3:c.2084C>T	NP_001122082.1:p.Thr695Ile
NM_001283049.2:c.1766C>T	NP_001269978.1:p.Thr589Ile