Canonical Allele Identifier: CA1713890133
Gene: GUSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65981849_65981850delinsAC , CM000669.2:g.65981849_65981850delinsAC GRCh38
NC_000007.13:g.65446836_65446837delinsAC , CM000669.1:g.65446836_65446837delinsAC GRCh37
NC_000007.12:g.65084271_65084272delinsAC NCBI36
NG_016197.1:g.5465_5466delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.210+124_210+125delinsGT MANE Select ENSP00000302728.4:n.210+124_210+125delinsGT
ENST00000304895.8:c.210+124_210+125delinsGT ENSP00000302728.4:n.210+124_210+125delinsGT
ENST00000421103.5:c.210+124_210+125delinsGT ENSP00000391390.1:n.210+124_210+125delinsGT
ENST00000430730.5:c.210+124_210+125delinsGT ENSP00000411859.1:n.210+124_210+125delinsGT
ENST00000446111.1:c.210+124_210+125delinsGT ENSP00000416793.1:n.210+124_210+125delinsGT
ENST00000447929.5:c.210+124_210+125delinsGT ENSP00000411262.1:n.210+124_210+125delinsGT
ENST00000475316.5:n.115+124_115+125delinsGT
ENST00000476486.5:n.121+1_121+2delinsGT
NM_000181.3:c.210+124_210+125delinsGT NP_000172.2:n.210+124_210+125delinsGT
NM_001284290.1:c.210+124_210+125delinsGT NP_001271219.1:n.210+124_210+125delinsGT
NM_001293104.1:c.-176+124_-176+125delinsGT NP_001280033.1:n.-176+124_-176+125delinsGT
NM_001293105.1:c.-120+124_-120+125delinsGT NP_001280034.1:n.-120+124_-120+125delinsGT
NR_120531.1:n.341+124_341+125delinsGT
XM_005250297.3:c.210+124_210+125delinsGT XP_005250354.1:n.210+124_210+125delinsGT
XM_011516113.1:c.-120+124_-120+125delinsGT XP_011514415.1:n.-120+124_-120+125delinsGT
XR_927461.1:n.336+124_336+125delinsGT
XM_005250297.4:c.210+124_210+125delinsGT XP_005250354.1:n.210+124_210+125delinsGT
XM_011516114.2:c.-476+124_-476+125delinsGT XP_011514416.1:n.-476+124_-476+125delinsGT
XM_017012091.1:c.-120+124_-120+125delinsGT XP_016867580.1:n.-120+124_-120+125delinsGT
XM_017012092.1:c.-176+124_-176+125delinsGT XP_016867581.1:n.-176+124_-176+125delinsGT
XM_017012093.2:c.-476+124_-476+125delinsGT XP_016867582.1:n.-476+124_-476+125delinsGT
XR_001744658.2:n.255+124_255+125delinsGT
XR_001744659.2:n.255+124_255+125delinsGT
XR_001744660.2:n.255+124_255+125delinsGT
XR_001744661.2:n.255+124_255+125delinsGT
XR_927461.3:n.255+124_255+125delinsGT
NM_000181.4:c.210+124_210+125delinsGT MANE Select NP_000172.2:n.210+124_210+125delinsGT
NM_001284290.2:c.210+124_210+125delinsGT NP_001271219.1:n.210+124_210+125delinsGT
NM_001293104.2:c.-176+124_-176+125delinsGT NP_001280033.1:n.-176+124_-176+125delinsGT
NM_001293105.2:c.-120+124_-120+125delinsGT NP_001280034.1:n.-120+124_-120+125delinsGT
NR_120531.2:n.240+124_240+125delinsGT