Canonical Allele Identifier: CA2590115247
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6696079_6696080insTCT , CM000679.2:g.6696079_6696080insTCT GRCh38
NC_000017.10:g.6599398_6599399insTCT , CM000679.1:g.6599398_6599399insTCT GRCh37
NC_000017.9:g.6540122_6540123insTCT NCBI36
NG_034220.1:g.22342_22343insAGA , LRG_1020:g.22342_22343insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.840-139_840-138insAGA MANE Select ENSP00000406220.2:n.840-139_840-138insAGA
ENST00000293800.10:c.789-139_789-138insAGA ENSP00000293800.6:n.789-139_789-138insAGA
ENST00000381074.8:c.711-139_711-138insAGA ENSP00000370464.4:n.711-139_711-138insAGA
ENST00000433363.6:c.840-139_840-138insAGA ENSP00000406220.2:n.840-139_840-138insAGA
ENST00000572094.1:c.*590-139_*590-138insAGA ENSP00000461495.1:n.*590-139_*590-138insAGA
ENST00000573648.5:c.840-139_840-138insAGA ENSP00000459372.1:n.840-139_840-138insAGA
ENST00000574824.5:n.1973-139_1973-138insAGA
NM_001143838.2:c.840-139_840-138insAGA NP_001137310.1:n.840-139_840-138insAGA
NM_001284509.1:c.789-139_789-138insAGA NP_001271438.1:n.789-139_789-138insAGA
NM_001284510.1:c.711-139_711-138insAGA NP_001271439.1:n.711-139_711-138insAGA
NM_177550.4:c.840-139_840-138insAGA , LRG_1020t1:c.840-139_840-138insAGA NP_808218.1:n.840-139_840-138insAGA
XM_006721504.2:c.729-139_729-138insAGA XP_006721567.1:n.729-139_729-138insAGA
XM_011523795.1:c.840-139_840-138insAGA XP_011522097.1:n.840-139_840-138insAGA
XM_011523795.3:c.840-139_840-138insAGA XP_011522097.1:n.840-139_840-138insAGA
NM_001143838.3:c.840-139_840-138insAGA NP_001137310.1:n.840-139_840-138insAGA
NM_001284509.2:c.789-139_789-138insAGA NP_001271438.1:n.789-139_789-138insAGA
NM_001284510.2:c.711-139_711-138insAGA NP_001271439.1:n.711-139_711-138insAGA
NM_177550.5:c.840-139_840-138insAGA MANE Select NP_808218.1:n.840-139_840-138insAGA