Canonical Allele Identifier: CA1713854392
Gene: GUSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65960901G= , CM000669.2:g.65960901G= GRCh38
NC_000007.13:g.65425888G= , CM000669.1:g.65425888G= GRCh37
NC_000007.12:g.65063323G= NCBI36
NG_016197.1:g.26414C=
NG_051954.1:g.92803G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304895.9:c.1952C= MANE Select ENSP00000302728.4:p.Thr651=
ENST00000304895.8:c.1952C= ENSP00000302728.4:p.Thr651=
ENST00000421103.5:c.1514C= ENSP00000391390.1:p.Thr505=
ENST00000430730.5:c.*1219C= ENSP00000411859.1:n.*1219C=
ENST00000447929.5:c.*1332C= ENSP00000411262.1:n.*1332C=
ENST00000466883.5:n.2342C=
NM_000181.3:c.1952C= NP_000172.2:p.Thr651=
NM_001284290.1:c.1514C= NP_001271219.1:p.Thr505=
NM_001293104.1:c.1382C= NP_001280033.1:p.Thr461=
NM_001293105.1:c.1295C= NP_001280034.1:p.Thr432=
NR_120531.1:n.1998C=
XM_005250297.3:c.1799C= XP_005250354.1:p.Thr600=
XM_011516113.1:c.1451C= XP_011514415.1:p.Thr484=
XM_011516114.1:c.1280C= XP_011514416.1:p.Thr427=
XM_005250297.4:c.1799C= XP_005250354.1:p.Thr600=
XM_011516114.2:c.1280C= XP_011514416.1:p.Thr427=
XM_017012091.1:c.1298C= XP_016867580.1:p.Thr433=
XM_017012092.1:c.1229C= XP_016867581.1:p.Thr410=
XM_017012093.2:c.1127C= XP_016867582.1:p.Thr376=
XR_001744658.2:n.1759C=
XR_001744659.2:n.1872C=
XR_001744660.2:n.1804C=
XR_001744661.2:n.1719C=
XR_927461.3:n.1957C=
NM_000181.4:c.1952C= MANE Select NP_000172.2:p.Thr651=
NM_001284290.2:c.1514C= NP_001271219.1:p.Thr505=
NM_001293104.2:c.1382C= NP_001280033.1:p.Thr461=
NM_001293105.2:c.1295C= NP_001280034.1:p.Thr432=
NR_120531.2:n.1897C=