Canonical Allele Identifier: CA575259331
Gene: GUSB HGNC NCBI

Linked Data

dbSNP Id: rs1377855703

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65982123_65982135del , CM000669.2:g.65982123_65982135del GRCh38
NC_000007.13:g.65447110_65447122del , CM000669.1:g.65447110_65447122del GRCh37
NC_000007.12:g.65084545_65084557del NCBI36
NG_016197.1:g.5189_5201del

Transcript Alleles

HGVS Amino-acid change
ENST00000304895.9:c.58_70del MANE Select ENSP00000302728.4:p.Ala20ArgfsTer?
ENST00000304895.8:c.58_70del ENSP00000302728.4:p.Ala20ArgfsTer?
ENST00000421103.5:c.58_70del ENSP00000391390.1:p.Ala20ArgfsTer?
ENST00000430730.5:c.58_70del ENSP00000411859.1:p.Ala20ArgfsTer?
ENST00000446111.1:c.58_70del ENSP00000416793.1:p.Ala20ArgfsTer?
ENST00000447929.5:c.58_70del ENSP00000411262.1:p.Ala20ArgfsTer?
NM_000181.3:c.58_70del NP_000172.2:p.Ala20ArgfsTer?
NM_001284290.1:c.58_70del NP_001271219.1:p.Ala20ArgfsTer?
NM_001293104.1:c.-328_-316del NP_001280033.1:n.-328_-316del
NM_001293105.1:c.-272_-260del NP_001280034.1:n.-272_-260del
NR_120531.1:n.189_201del
XM_005250297.3:c.58_70del XP_005250354.1:p.Ala20ArgfsTer?
XM_011516113.1:c.-272_-260del XP_011514415.1:n.-272_-260del
XR_927461.1:n.184_196del
XM_005250297.4:c.58_70del XP_005250354.1:p.Ala20ArgfsTer?
XM_011516114.2:c.-628_-616del XP_011514416.1:n.-628_-616del
XM_017012091.1:c.-272_-260del XP_016867580.1:n.-272_-260del
XM_017012092.1:c.-328_-316del XP_016867581.1:n.-328_-316del
XM_017012093.2:c.-628_-616del XP_016867582.1:n.-628_-616del
XR_001744658.2:n.103_115del
XR_001744659.2:n.103_115del
XR_001744660.2:n.103_115del
XR_001744661.2:n.103_115del
XR_927461.3:n.103_115del
NM_000181.4:c.58_70del MANE Select NP_000172.2:p.Ala20ArgfsTer?
NM_001284290.2:c.58_70del NP_001271219.1:p.Ala20ArgfsTer?
NM_001293104.2:c.-328_-316del NP_001280033.1:n.-328_-316del
NM_001293105.2:c.-272_-260del NP_001280034.1:n.-272_-260del
NR_120531.2:n.88_100del