Canonical Allele Identifier: CA2245459115
Gene: SLC13A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703084C= , CM000679.2:g.6703084C= GRCh38
NC_000017.10:g.6606403C= , CM000679.1:g.6606403C= GRCh37
NC_000017.9:g.6547127C= NCBI36
NG_034220.1:g.15338G= , LRG_1020:g.15338G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.602G= MANE Select ENSP00000406220.2:p.Arg201=
ENST00000293800.10:c.551G= ENSP00000293800.6:p.Arg184=
ENST00000381074.8:c.473G= ENSP00000370464.4:p.Arg158=
ENST00000433363.6:c.602G= ENSP00000406220.2:p.Arg201=
ENST00000572094.1:c.*352G= ENSP00000461495.1:n.*352G=
ENST00000572352.5:c.491G= ENSP00000461622.1:p.Arg164=
ENST00000573648.5:c.602G= ENSP00000459372.1:p.Arg201=
ENST00000574824.5:n.1735G=
NM_001143838.2:c.602G= NP_001137310.1:p.Arg201=
NM_001284509.1:c.551G= NP_001271438.1:p.Arg184=
NM_001284510.1:c.473G= NP_001271439.1:p.Arg158=
NM_177550.4:c.602G= , LRG_1020t1:c.602G= NP_808218.1:p.Arg201=
XM_006721504.2:c.491G= XP_006721567.1:p.Arg164=
XM_011523795.1:c.602G= XP_011522097.1:p.Arg201=
XM_011523795.3:c.602G= XP_011522097.1:p.Arg201=
NM_001143838.3:c.602G= NP_001137310.1:p.Arg201=
NM_001284509.2:c.551G= NP_001271438.1:p.Arg184=
NM_001284510.2:c.473G= NP_001271439.1:p.Arg158=
NM_177550.5:c.602G= MANE Select NP_808218.1:p.Arg201=