Canonical Allele Identifier: CA8331643
Gene: SLC13A5 HGNC NCBI

Linked Data

dbSNP Id: rs749718065
gnomAD v2: 17-6606310-A-G
gnomAD v4: 17-6702991-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6702991A>G , CM000679.2:g.6702991A>G GRCh38
NC_000017.10:g.6606310A>G , CM000679.1:g.6606310A>G GRCh37
NC_000017.9:g.6547034A>G NCBI36
NG_034220.1:g.15431T>C , LRG_1020:g.15431T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.695T>C MANE Select ENSP00000406220.2:p.Val232Ala
ENST00000293800.10:c.644T>C ENSP00000293800.6:p.Val215Ala
ENST00000381074.8:c.566T>C ENSP00000370464.4:p.Val189Ala
ENST00000433363.6:c.695T>C ENSP00000406220.2:p.Val232Ala
ENST00000572094.1:c.*445T>C ENSP00000461495.1:n.*445T>C
ENST00000573648.5:c.695T>C ENSP00000459372.1:p.Val232Ala
ENST00000574824.5:n.1828T>C
NM_001143838.2:c.695T>C NP_001137310.1:p.Val232Ala
NM_001284509.1:c.644T>C NP_001271438.1:p.Val215Ala
NM_001284510.1:c.566T>C NP_001271439.1:p.Val189Ala
NM_177550.4:c.695T>C , LRG_1020t1:c.695T>C NP_808218.1:p.Val232Ala
XM_006721504.2:c.584T>C XP_006721567.1:p.Val195Ala
XM_011523795.1:c.695T>C XP_011522097.1:p.Val232Ala
XM_011523795.3:c.695T>C XP_011522097.1:p.Val232Ala
NM_001143838.3:c.695T>C NP_001137310.1:p.Val232Ala
NM_001284509.2:c.644T>C NP_001271438.1:p.Val215Ala
NM_001284510.2:c.566T>C NP_001271439.1:p.Val189Ala
NM_177550.5:c.695T>C MANE Select NP_808218.1:p.Val232Ala