Canonical Allele Identifier: CA367637597
Gene: GUSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65961039T>C , CM000669.2:g.65961039T>C GRCh38
NC_000007.13:g.65426026T>C , CM000669.1:g.65426026T>C GRCh37
NC_000007.12:g.65063461T>C NCBI36
NG_016197.1:g.26276A>G
NG_051954.1:g.92941T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.1814A>G MANE Select ENSP00000302728.4:p.Lys605Arg
ENST00000304895.8:c.1814A>G ENSP00000302728.4:p.Lys605Arg
ENST00000421103.5:c.1376A>G ENSP00000391390.1:p.Lys459Arg
ENST00000430730.5:c.*1081A>G ENSP00000411859.1:n.*1081A>G
ENST00000447929.5:c.*1194A>G ENSP00000411262.1:n.*1194A>G
ENST00000466883.5:n.2204A>G
NM_000181.3:c.1814A>G NP_000172.2:p.Lys605Arg
NM_001284290.1:c.1376A>G NP_001271219.1:p.Lys459Arg
NM_001293104.1:c.1244A>G NP_001280033.1:p.Lys415Arg
NM_001293105.1:c.1157A>G NP_001280034.1:p.Lys386Arg
NR_120531.1:n.1860A>G
XM_005250297.3:c.1661A>G XP_005250354.1:p.Lys554Arg
XM_011516113.1:c.1313A>G XP_011514415.1:p.Lys438Arg
XM_011516114.1:c.1142A>G XP_011514416.1:p.Lys381Arg
XM_005250297.4:c.1661A>G XP_005250354.1:p.Lys554Arg
XM_011516114.2:c.1142A>G XP_011514416.1:p.Lys381Arg
XM_017012091.1:c.1160A>G XP_016867580.1:p.Lys387Arg
XM_017012092.1:c.1091A>G XP_016867581.1:p.Lys364Arg
XM_017012093.2:c.989A>G XP_016867582.1:p.Lys330Arg
XR_001744658.2:n.1621A>G
XR_001744659.2:n.1734A>G
XR_001744660.2:n.1666A>G
XR_001744661.2:n.1581A>G
XR_927461.3:n.1819A>G
NM_000181.4:c.1814A>G MANE Select NP_000172.2:p.Lys605Arg
NM_001284290.2:c.1376A>G NP_001271219.1:p.Lys459Arg
NM_001293104.2:c.1244A>G NP_001280033.1:p.Lys415Arg
NM_001293105.2:c.1157A>G NP_001280034.1:p.Lys386Arg
NR_120531.2:n.1759A>G