Canonical Allele Identifier: CA5279571

Gene: USP20

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129868444C>T , CM000671.2:g.129868444C>T	GRCh38
NC_000009.11:g.132630723C>T , CM000671.1:g.132630723C>T	GRCh37
NC_000009.10:g.131670544C>T	NCBI36
NG_033097.1:g.38028C>T
NG_033097.2:g.38016C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315480.9:c.1130C>T	ENSP00000313811.4:p.Thr377Met
ENST00000372429.8:c.1130C>T MANE Select	ENSP00000361506.3:p.Thr377Met
ENST00000315480.8:c.1130C>T	ENSP00000313811.4:p.Thr377Met
ENST00000358355.5:c.1130C>T	ENSP00000351122.1:p.Thr377Met
ENST00000372429.7:c.1130C>T	ENSP00000361506.3:p.Thr377Met
ENST00000474895.6:n.123C>T
ENST00000491731.1:n.78C>T
NM_001008563.4:c.1130C>T	NP_001008563.2:p.Thr377Met
NM_001110303.3:c.1130C>T	NP_001103773.2:p.Thr377Met
NM_006676.7:c.1130C>T	NP_006667.3:p.Thr377Met
XM_005251665.2:c.1130C>T	XP_005251722.1:p.Thr377Met
XM_005251666.2:c.413C>T	XP_005251723.1:p.Thr138Met
XM_011518161.1:c.1130C>T	XP_011516463.1:p.Thr377Met
XM_011518162.1:c.1130C>T	XP_011516464.1:p.Thr377Met
XM_005251665.3:c.1130C>T	XP_005251722.1:p.Thr377Met
XM_011518161.2:c.1130C>T	XP_011516463.1:p.Thr377Met
XM_011518162.2:c.1130C>T	XP_011516464.1:p.Thr377Met
XM_024447389.1:c.413C>T	XP_024303157.1:p.Thr138Met
XM_024447390.1:c.413C>T	XP_024303158.1:p.Thr138Met
NM_001110303.4:c.1130C>T MANE Select	NP_001103773.2:p.Thr377Met
NM_001008563.5:c.1130C>T	NP_001008563.2:p.Thr377Met
NM_006676.8:c.1130C>T	NP_006667.3:p.Thr377Met