Canonical Allele Identifier: CA397749949
Gene: SLC13A5 HGNC NCBI

Linked Data

gnomAD v4: 17-6703901-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703901T>G , CM000679.2:g.6703901T>G GRCh38
NC_000017.10:g.6607220T>G , CM000679.1:g.6607220T>G GRCh37
NC_000017.9:g.6547944T>G NCBI36
NG_034220.1:g.14521A>C , LRG_1020:g.14521A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.524A>C MANE Select ENSP00000406220.2:p.Lys175Thr
ENST00000293800.10:c.473A>C ENSP00000293800.6:p.Lys158Thr
ENST00000381074.8:c.395A>C ENSP00000370464.4:p.Lys132Thr
ENST00000433363.6:c.524A>C ENSP00000406220.2:p.Lys175Thr
ENST00000572094.1:c.*274A>C ENSP00000461495.1:n.*274A>C
ENST00000572352.5:c.413A>C ENSP00000461622.1:p.Lys138Thr
ENST00000573648.5:c.524A>C ENSP00000459372.1:p.Lys175Thr
ENST00000574824.5:n.1657A>C
ENST00000576323.1:n.554A>C
NM_001143838.2:c.524A>C NP_001137310.1:p.Lys175Thr
NM_001284509.1:c.473A>C NP_001271438.1:p.Lys158Thr
NM_001284510.1:c.395A>C NP_001271439.1:p.Lys132Thr
NM_177550.4:c.524A>C , LRG_1020t1:c.524A>C NP_808218.1:p.Lys175Thr
XM_006721504.2:c.413A>C XP_006721567.1:p.Lys138Thr
XM_011523795.1:c.524A>C XP_011522097.1:p.Lys175Thr
XM_011523795.3:c.524A>C XP_011522097.1:p.Lys175Thr
NM_001143838.3:c.524A>C NP_001137310.1:p.Lys175Thr
NM_001284509.2:c.473A>C NP_001271438.1:p.Lys158Thr
NM_001284510.2:c.395A>C NP_001271439.1:p.Lys132Thr
NM_177550.5:c.524A>C MANE Select NP_808218.1:p.Lys175Thr