Canonical Allele Identifier: CA2245460128
Gene: SLC13A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703921G= , CM000679.2:g.6703921G= GRCh38
NC_000017.10:g.6607240G= , CM000679.1:g.6607240G= GRCh37
NC_000017.9:g.6547964G= NCBI36
NG_034220.1:g.14501C= , LRG_1020:g.14501C=

Transcript Alleles

HGVS Amino-acid change
ENST00000433363.7:c.504C= MANE Select ENSP00000406220.2:p.Ala168=
ENST00000293800.10:c.453C= ENSP00000293800.6:p.Ala151=
ENST00000381074.8:c.375C= ENSP00000370464.4:p.Ala125=
ENST00000433363.6:c.504C= ENSP00000406220.2:p.Ala168=
ENST00000572094.1:c.*254C= ENSP00000461495.1:n.*254C=
ENST00000572352.5:c.393C= ENSP00000461622.1:p.Ala131=
ENST00000573648.5:c.504C= ENSP00000459372.1:p.Ala168=
ENST00000574824.5:n.1637C=
ENST00000576323.1:n.534C=
NM_001143838.2:c.504C= NP_001137310.1:p.Ala168=
NM_001284509.1:c.453C= NP_001271438.1:p.Ala151=
NM_001284510.1:c.375C= NP_001271439.1:p.Ala125=
NM_177550.4:c.504C= , LRG_1020t1:c.504C= NP_808218.1:p.Ala168=
XM_006721504.2:c.393C= XP_006721567.1:p.Ala131=
XM_011523795.1:c.504C= XP_011522097.1:p.Ala168=
XM_011523795.3:c.504C= XP_011522097.1:p.Ala168=
NM_001143838.3:c.504C= NP_001137310.1:p.Ala168=
NM_001284509.2:c.453C= NP_001271438.1:p.Ala151=
NM_001284510.2:c.375C= NP_001271439.1:p.Ala125=
NM_177550.5:c.504C= MANE Select NP_808218.1:p.Ala168=