Canonical Allele Identifier: CA1713854383
Gene: GUSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65960897T= , CM000669.2:g.65960897T= GRCh38
NC_000007.13:g.65425884T= , CM000669.1:g.65425884T= GRCh37
NC_000007.12:g.65063319T= NCBI36
NG_016197.1:g.26418A=
NG_051954.1:g.92799T=

Transcript Alleles

HGVS Amino-acid change
ENST00000304895.9:c.1956A= MANE Select ENSP00000302728.4:p.Ter652=
ENST00000304895.8:c.1956A= ENSP00000302728.4:p.Ter652=
ENST00000421103.5:c.1518A= ENSP00000391390.1:p.Ter506=
ENST00000430730.5:c.*1223A= ENSP00000411859.1:n.*1223A=
ENST00000447929.5:c.*1336A= ENSP00000411262.1:n.*1336A=
ENST00000466883.5:n.2346A=
NM_000181.3:c.1956A= NP_000172.2:p.Ter652=
NM_001284290.1:c.1518A= NP_001271219.1:p.Ter506=
NM_001293104.1:c.1386A= NP_001280033.1:p.Ter462=
NM_001293105.1:c.1299A= NP_001280034.1:p.Ter433=
NR_120531.1:n.2002A=
XM_005250297.3:c.1803A= XP_005250354.1:p.Ter601=
XM_011516113.1:c.1455A= XP_011514415.1:p.Ter485=
XM_011516114.1:c.1284A= XP_011514416.1:p.Ter428=
XM_005250297.4:c.1803A= XP_005250354.1:p.Ter601=
XM_011516114.2:c.1284A= XP_011514416.1:p.Ter428=
XM_017012091.1:c.1302A= XP_016867580.1:p.Ter434=
XM_017012092.1:c.1233A= XP_016867581.1:p.Ter411=
XM_017012093.2:c.1131A= XP_016867582.1:p.Ter377=
XR_001744658.2:n.1763A=
XR_001744659.2:n.1876A=
XR_001744660.2:n.1808A=
XR_001744661.2:n.1723A=
XR_927461.3:n.1961A=
NM_000181.4:c.1956A= MANE Select NP_000172.2:p.Ter652=
NM_001284290.2:c.1518A= NP_001271219.1:p.Ter506=
NM_001293104.2:c.1386A= NP_001280033.1:p.Ter462=
NM_001293105.2:c.1299A= NP_001280034.1:p.Ter433=
NR_120531.2:n.1901A=