Canonical Allele Identifier: CA397749939
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703896T>G , CM000679.2:g.6703896T>G GRCh38
NC_000017.10:g.6607215T>G , CM000679.1:g.6607215T>G GRCh37
NC_000017.9:g.6547939T>G NCBI36
NG_034220.1:g.14526A>C , LRG_1020:g.14526A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.529A>C MANE Select ENSP00000406220.2:p.Lys177Gln
ENST00000293800.10:c.478A>C ENSP00000293800.6:p.Lys160Gln
ENST00000381074.8:c.400A>C ENSP00000370464.4:p.Lys134Gln
ENST00000433363.6:c.529A>C ENSP00000406220.2:p.Lys177Gln
ENST00000572094.1:c.*279A>C ENSP00000461495.1:n.*279A>C
ENST00000572352.5:c.418A>C ENSP00000461622.1:p.Lys140Gln
ENST00000573648.5:c.529A>C ENSP00000459372.1:p.Lys177Gln
ENST00000574824.5:n.1662A>C
ENST00000576323.1:n.559A>C
NM_001143838.2:c.529A>C NP_001137310.1:p.Lys177Gln
NM_001284509.1:c.478A>C NP_001271438.1:p.Lys160Gln
NM_001284510.1:c.400A>C NP_001271439.1:p.Lys134Gln
NM_177550.4:c.529A>C , LRG_1020t1:c.529A>C NP_808218.1:p.Lys177Gln
XM_006721504.2:c.418A>C XP_006721567.1:p.Lys140Gln
XM_011523795.1:c.529A>C XP_011522097.1:p.Lys177Gln
XM_011523795.3:c.529A>C XP_011522097.1:p.Lys177Gln
NM_001143838.3:c.529A>C NP_001137310.1:p.Lys177Gln
NM_001284509.2:c.478A>C NP_001271438.1:p.Lys160Gln
NM_001284510.2:c.400A>C NP_001271439.1:p.Lys134Gln
NM_177550.5:c.529A>C MANE Select NP_808218.1:p.Lys177Gln