Canonical Allele Identifier: CA981132630
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6696067_6696068insAC , CM000679.2:g.6696067_6696068insAC GRCh38
NC_000017.10:g.6599386_6599387insAC , CM000679.1:g.6599386_6599387insAC GRCh37
NC_000017.9:g.6540110_6540111insAC NCBI36
NG_034220.1:g.22354_22355insGT , LRG_1020:g.22354_22355insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.840-127_840-126insGT MANE Select ENSP00000406220.2:n.840-127_840-126insGT
ENST00000293800.10:c.789-127_789-126insGT ENSP00000293800.6:n.789-127_789-126insGT
ENST00000381074.8:c.711-127_711-126insGT ENSP00000370464.4:n.711-127_711-126insGT
ENST00000433363.6:c.840-127_840-126insGT ENSP00000406220.2:n.840-127_840-126insGT
ENST00000572094.1:c.*590-127_*590-126insGT ENSP00000461495.1:n.*590-127_*590-126insGT
ENST00000573648.5:c.840-127_840-126insGT ENSP00000459372.1:n.840-127_840-126insGT
ENST00000574824.5:n.1973-127_1973-126insGT
NM_001143838.2:c.840-127_840-126insGT NP_001137310.1:n.840-127_840-126insGT
NM_001284509.1:c.789-127_789-126insGT NP_001271438.1:n.789-127_789-126insGT
NM_001284510.1:c.711-127_711-126insGT NP_001271439.1:n.711-127_711-126insGT
NM_177550.4:c.840-127_840-126insGT , LRG_1020t1:c.840-127_840-126insGT NP_808218.1:n.840-127_840-126insGT
XM_006721504.2:c.729-127_729-126insGT XP_006721567.1:n.729-127_729-126insGT
XM_011523795.1:c.840-127_840-126insGT XP_011522097.1:n.840-127_840-126insGT
XM_011523795.3:c.840-127_840-126insGT XP_011522097.1:n.840-127_840-126insGT
NM_001143838.3:c.840-127_840-126insGT NP_001137310.1:n.840-127_840-126insGT
NM_001284509.2:c.789-127_789-126insGT NP_001271438.1:n.789-127_789-126insGT
NM_001284510.2:c.711-127_711-126insGT NP_001271439.1:n.711-127_711-126insGT
NM_177550.5:c.840-127_840-126insGT MANE Select NP_808218.1:n.840-127_840-126insGT