Canonical Allele Identifier: CA377910492
Community Standard Title: NM_016169.4(SUFU):c.825G>A (p.Trp275Ter)
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102597208G>A , CM000672.2:g.102597208G>A GRCh38
NC_000010.10:g.104356965G>A , CM000672.1:g.104356965G>A GRCh37
NC_000010.9:g.104346955G>A NCBI36
NG_021338.1:g.98247G>A , LRG_521:g.98247G>A

Transcript Alleles

HGVS Amino-acid Change
NM_016169.4:c.825G>A MANE Select NP_057253.2:p.Trp275Ter
ENST00000369902.8:c.825G>A MANE Select ENSP00000358918.4:p.Trp275Ter
NM_001178133.1:c.825G>A NP_001171604.1:p.Trp275Ter
NM_001178133.2:c.825G>A NP_001171604.1:p.Trp275Ter
NM_016169.3:c.825G>A , LRG_521t1:c.825G>A NP_057253.2:p.Trp275Ter
ENST00000369899.6:c.825G>A ENSP00000358915.2:p.Trp275Ter
ENST00000369902.7:c.825G>A ENSP00000358918.3:p.Trp275Ter
ENST00000423559.2:c.825G>A ENSP00000411597.2:p.Trp275Ter
ENST00000471000.1:n.607G>A
XM_011539858.1:c.828G>A XP_011538160.1:p.Trp276Ter
XM_011539858.3:c.828G>A XP_011538160.1:p.Trp276Ter
XM_011539859.1:c.828G>A XP_011538161.1:p.Trp276Ter
XM_011539860.1:c.825G>A XP_011538162.1:p.Trp275Ter
XM_011539860.3:c.825G>A XP_011538162.1:p.Trp275Ter
XM_011539861.1:c.828G>A XP_011538163.1:p.Trp276Ter
XM_011539861.3:c.828G>A XP_011538163.1:p.Trp276Ter
XM_011539862.1:c.750G>A XP_011538164.1:p.Trp250Ter
XM_011539863.1:c.654G>A XP_011538165.1:p.Trp218Ter
XM_011539863.3:c.654G>A XP_011538165.1:p.Trp218Ter
XM_011539864.1:c.828G>A XP_011538166.1:p.Trp276Ter
XM_011539864.3:c.828G>A XP_011538166.1:p.Trp276Ter
XM_017016323.1:c.750G>A XP_016871812.1:p.Trp250Ter