Canonical Allele Identifier: CA367637589
Gene: GUSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65961037T>G , CM000669.2:g.65961037T>G GRCh38
NC_000007.13:g.65426024T>G , CM000669.1:g.65426024T>G GRCh37
NC_000007.12:g.65063459T>G NCBI36
NG_016197.1:g.26278A>C
NG_051954.1:g.92939T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.1816A>C MANE Select ENSP00000302728.4:p.Lys606Gln
ENST00000304895.8:c.1816A>C ENSP00000302728.4:p.Lys606Gln
ENST00000421103.5:c.1378A>C ENSP00000391390.1:p.Lys460Gln
ENST00000430730.5:c.*1083A>C ENSP00000411859.1:n.*1083A>C
ENST00000447929.5:c.*1196A>C ENSP00000411262.1:n.*1196A>C
ENST00000466883.5:n.2206A>C
NM_000181.3:c.1816A>C NP_000172.2:p.Lys606Gln
NM_001284290.1:c.1378A>C NP_001271219.1:p.Lys460Gln
NM_001293104.1:c.1246A>C NP_001280033.1:p.Lys416Gln
NM_001293105.1:c.1159A>C NP_001280034.1:p.Lys387Gln
NR_120531.1:n.1862A>C
XM_005250297.3:c.1663A>C XP_005250354.1:p.Lys555Gln
XM_011516113.1:c.1315A>C XP_011514415.1:p.Lys439Gln
XM_011516114.1:c.1144A>C XP_011514416.1:p.Lys382Gln
XM_005250297.4:c.1663A>C XP_005250354.1:p.Lys555Gln
XM_011516114.2:c.1144A>C XP_011514416.1:p.Lys382Gln
XM_017012091.1:c.1162A>C XP_016867580.1:p.Lys388Gln
XM_017012092.1:c.1093A>C XP_016867581.1:p.Lys365Gln
XM_017012093.2:c.991A>C XP_016867582.1:p.Lys331Gln
XR_001744658.2:n.1623A>C
XR_001744659.2:n.1736A>C
XR_001744660.2:n.1668A>C
XR_001744661.2:n.1583A>C
XR_927461.3:n.1821A>C
NM_000181.4:c.1816A>C MANE Select NP_000172.2:p.Lys606Gln
NM_001284290.2:c.1378A>C NP_001271219.1:p.Lys460Gln
NM_001293104.2:c.1246A>C NP_001280033.1:p.Lys416Gln
NM_001293105.2:c.1159A>C NP_001280034.1:p.Lys387Gln
NR_120531.2:n.1761A>C