Canonical Allele Identifier: CA367637595
Gene: GUSB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000304895.9:c.1814A>T MANE Select ENSP00000302728.4:p.Lys605Ile
ENST00000304895.8:c.1814A>T ENSP00000302728.4:p.Lys605Ile
ENST00000421103.5:c.1376A>T ENSP00000391390.1:p.Lys459Ile
ENST00000430730.5:c.*1081A>T ENSP00000411859.1:n.*1081A>T
ENST00000447929.5:c.*1194A>T ENSP00000411262.1:n.*1194A>T
ENST00000466883.5:n.2204A>T
NM_000181.3:c.1814A>T NP_000172.2:p.Lys605Ile
NM_001284290.1:c.1376A>T NP_001271219.1:p.Lys459Ile
NM_001293104.1:c.1244A>T NP_001280033.1:p.Lys415Ile
NM_001293105.1:c.1157A>T NP_001280034.1:p.Lys386Ile
NR_120531.1:n.1860A>T
XM_005250297.3:c.1661A>T XP_005250354.1:p.Lys554Ile
XM_011516113.1:c.1313A>T XP_011514415.1:p.Lys438Ile
XM_011516114.1:c.1142A>T XP_011514416.1:p.Lys381Ile
XM_005250297.4:c.1661A>T XP_005250354.1:p.Lys554Ile
XM_011516114.2:c.1142A>T XP_011514416.1:p.Lys381Ile
XM_017012091.1:c.1160A>T XP_016867580.1:p.Lys387Ile
XM_017012092.1:c.1091A>T XP_016867581.1:p.Lys364Ile
XM_017012093.2:c.989A>T XP_016867582.1:p.Lys330Ile
XR_001744658.2:n.1621A>T
XR_001744659.2:n.1734A>T
XR_001744660.2:n.1666A>T
XR_001744661.2:n.1581A>T
XR_927461.3:n.1819A>T
NM_000181.4:c.1814A>T MANE Select NP_000172.2:p.Lys605Ile
NM_001284290.2:c.1376A>T NP_001271219.1:p.Lys459Ile
NM_001293104.2:c.1244A>T NP_001280033.1:p.Lys415Ile
NM_001293105.2:c.1157A>T NP_001280034.1:p.Lys386Ile
NR_120531.2:n.1759A>T