Canonical Allele Identifier: CA981132733
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6696077_6696087del , CM000679.2:g.6696077_6696087del GRCh38
NC_000017.10:g.6599396_6599406del , CM000679.1:g.6599396_6599406del GRCh37
NC_000017.9:g.6540120_6540130del NCBI36
NG_034220.1:g.22335_22345del , LRG_1020:g.22335_22345del

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.840-146_840-136del MANE Select ENSP00000406220.2:n.840-146_840-136del
ENST00000293800.10:c.789-146_789-136del ENSP00000293800.6:n.789-146_789-136del
ENST00000381074.8:c.711-146_711-136del ENSP00000370464.4:n.711-146_711-136del
ENST00000433363.6:c.840-146_840-136del ENSP00000406220.2:n.840-146_840-136del
ENST00000572094.1:c.*590-146_*590-136del ENSP00000461495.1:n.*590-146_*590-136del
ENST00000573648.5:c.840-146_840-136del ENSP00000459372.1:n.840-146_840-136del
ENST00000574824.5:n.1973-146_1973-136del
NM_001143838.2:c.840-146_840-136del NP_001137310.1:n.840-146_840-136del
NM_001284509.1:c.789-146_789-136del NP_001271438.1:n.789-146_789-136del
NM_001284510.1:c.711-146_711-136del NP_001271439.1:n.711-146_711-136del
NM_177550.4:c.840-146_840-136del , LRG_1020t1:c.840-146_840-136del NP_808218.1:n.840-146_840-136del
XM_006721504.2:c.729-146_729-136del XP_006721567.1:n.729-146_729-136del
XM_011523795.1:c.840-146_840-136del XP_011522097.1:n.840-146_840-136del
XM_011523795.3:c.840-146_840-136del XP_011522097.1:n.840-146_840-136del
NM_001143838.3:c.840-146_840-136del NP_001137310.1:n.840-146_840-136del
NM_001284509.2:c.789-146_789-136del NP_001271438.1:n.789-146_789-136del
NM_001284510.2:c.711-146_711-136del NP_001271439.1:n.711-146_711-136del
NM_177550.5:c.840-146_840-136del MANE Select NP_808218.1:n.840-146_840-136del