Canonical Allele Identifier: CA2245463852
Gene: SLC13A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6707303_6707304delinsTG , CM000679.2:g.6707303_6707304delinsTG GRCh38
NC_000017.10:g.6610622_6610623delinsTG , CM000679.1:g.6610622_6610623delinsTG GRCh37
NC_000017.9:g.6551346_6551347delinsTG NCBI36
NG_034220.1:g.11118_11119delinsCA , LRG_1020:g.11118_11119delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.103-148_103-147delinsCA MANE Select ENSP00000406220.2:n.103-148_103-147delinsCA
ENST00000293800.10:c.103-148_103-147delinsCA ENSP00000293800.6:n.103-148_103-147delinsCA
ENST00000381074.8:c.103-526_103-525delinsCA ENSP00000370464.4:n.103-526_103-525delinsCA
ENST00000433363.6:c.103-148_103-147delinsCA ENSP00000406220.2:n.103-148_103-147delinsCA
ENST00000572094.1:c.103-148_103-147delinsCA ENSP00000461495.1:n.103-148_103-147delinsCA
ENST00000572352.5:c.103-259_103-258delinsCA ENSP00000461622.1:n.103-259_103-258delinsCA
ENST00000573648.5:c.103-148_103-147delinsCA ENSP00000459372.1:n.103-148_103-147delinsCA
ENST00000575230.1:c.103-148_103-147delinsCA ENSP00000460903.1:n.103-148_103-147delinsCA
ENST00000576323.1:n.141-156_141-155delinsCA
NM_001143838.2:c.103-148_103-147delinsCA NP_001137310.1:n.103-148_103-147delinsCA
NM_001284509.1:c.103-148_103-147delinsCA NP_001271438.1:n.103-148_103-147delinsCA
NM_001284510.1:c.103-526_103-525delinsCA NP_001271439.1:n.103-526_103-525delinsCA
NM_177550.4:c.103-148_103-147delinsCA , LRG_1020t1:c.103-148_103-147delinsCA NP_808218.1:n.103-148_103-147delinsCA
XM_006721504.2:c.103-259_103-258delinsCA XP_006721567.1:n.103-259_103-258delinsCA
XM_011523795.1:c.103-148_103-147delinsCA XP_011522097.1:n.103-148_103-147delinsCA
XM_011523795.3:c.103-148_103-147delinsCA XP_011522097.1:n.103-148_103-147delinsCA
NM_001143838.3:c.103-148_103-147delinsCA NP_001137310.1:n.103-148_103-147delinsCA
NM_001284509.2:c.103-148_103-147delinsCA NP_001271438.1:n.103-148_103-147delinsCA
NM_001284510.2:c.103-526_103-525delinsCA NP_001271439.1:n.103-526_103-525delinsCA
NM_177550.5:c.103-148_103-147delinsCA MANE Select NP_808218.1:n.103-148_103-147delinsCA