Canonical Allele Identifier: CA367637060
Gene: GUSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65960931T>C , CM000669.2:g.65960931T>C GRCh38
NC_000007.13:g.65425918T>C , CM000669.1:g.65425918T>C GRCh37
NC_000007.12:g.65063353T>C NCBI36
NG_016197.1:g.26384A>G
NG_051954.1:g.92833T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.1922A>G MANE Select ENSP00000302728.4:p.Lys641Arg
ENST00000304895.8:c.1922A>G ENSP00000302728.4:p.Lys641Arg
ENST00000421103.5:c.1484A>G ENSP00000391390.1:p.Lys495Arg
ENST00000430730.5:c.*1189A>G ENSP00000411859.1:n.*1189A>G
ENST00000447929.5:c.*1302A>G ENSP00000411262.1:n.*1302A>G
ENST00000466883.5:n.2312A>G
NM_000181.3:c.1922A>G NP_000172.2:p.Lys641Arg
NM_001284290.1:c.1484A>G NP_001271219.1:p.Lys495Arg
NM_001293104.1:c.1352A>G NP_001280033.1:p.Lys451Arg
NM_001293105.1:c.1265A>G NP_001280034.1:p.Lys422Arg
NR_120531.1:n.1968A>G
XM_005250297.3:c.1769A>G XP_005250354.1:p.Lys590Arg
XM_011516113.1:c.1421A>G XP_011514415.1:p.Lys474Arg
XM_011516114.1:c.1250A>G XP_011514416.1:p.Lys417Arg
XM_005250297.4:c.1769A>G XP_005250354.1:p.Lys590Arg
XM_011516114.2:c.1250A>G XP_011514416.1:p.Lys417Arg
XM_017012091.1:c.1268A>G XP_016867580.1:p.Lys423Arg
XM_017012092.1:c.1199A>G XP_016867581.1:p.Lys400Arg
XM_017012093.2:c.1097A>G XP_016867582.1:p.Lys366Arg
XR_001744658.2:n.1729A>G
XR_001744659.2:n.1842A>G
XR_001744660.2:n.1774A>G
XR_001744661.2:n.1689A>G
XR_927461.3:n.1927A>G
NM_000181.4:c.1922A>G MANE Select NP_000172.2:p.Lys641Arg
NM_001284290.2:c.1484A>G NP_001271219.1:p.Lys495Arg
NM_001293104.2:c.1352A>G NP_001280033.1:p.Lys451Arg
NM_001293105.2:c.1265A>G NP_001280034.1:p.Lys422Arg
NR_120531.2:n.1867A>G