Canonical Allele Identifier: CA367637590
Gene: GUSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65961038T>A , CM000669.2:g.65961038T>A GRCh38
NC_000007.13:g.65426025T>A , CM000669.1:g.65426025T>A GRCh37
NC_000007.12:g.65063460T>A NCBI36
NG_016197.1:g.26277A>T
NG_051954.1:g.92940T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.1815A>T MANE Select ENSP00000302728.4:p.Lys605Asn
ENST00000304895.8:c.1815A>T ENSP00000302728.4:p.Lys605Asn
ENST00000421103.5:c.1377A>T ENSP00000391390.1:p.Lys459Asn
ENST00000430730.5:c.*1082A>T ENSP00000411859.1:n.*1082A>T
ENST00000447929.5:c.*1195A>T ENSP00000411262.1:n.*1195A>T
ENST00000466883.5:n.2205A>T
NM_000181.3:c.1815A>T NP_000172.2:p.Lys605Asn
NM_001284290.1:c.1377A>T NP_001271219.1:p.Lys459Asn
NM_001293104.1:c.1245A>T NP_001280033.1:p.Lys415Asn
NM_001293105.1:c.1158A>T NP_001280034.1:p.Lys386Asn
NR_120531.1:n.1861A>T
XM_005250297.3:c.1662A>T XP_005250354.1:p.Lys554Asn
XM_011516113.1:c.1314A>T XP_011514415.1:p.Lys438Asn
XM_011516114.1:c.1143A>T XP_011514416.1:p.Lys381Asn
XM_005250297.4:c.1662A>T XP_005250354.1:p.Lys554Asn
XM_011516114.2:c.1143A>T XP_011514416.1:p.Lys381Asn
XM_017012091.1:c.1161A>T XP_016867580.1:p.Lys387Asn
XM_017012092.1:c.1092A>T XP_016867581.1:p.Lys364Asn
XM_017012093.2:c.990A>T XP_016867582.1:p.Lys330Asn
XR_001744658.2:n.1622A>T
XR_001744659.2:n.1735A>T
XR_001744660.2:n.1667A>T
XR_001744661.2:n.1582A>T
XR_927461.3:n.1820A>T
NM_000181.4:c.1815A>T MANE Select NP_000172.2:p.Lys605Asn
NM_001284290.2:c.1377A>T NP_001271219.1:p.Lys459Asn
NM_001293104.2:c.1245A>T NP_001280033.1:p.Lys415Asn
NM_001293105.2:c.1158A>T NP_001280034.1:p.Lys386Asn
NR_120531.2:n.1760A>T