Canonical Allele Identifier: CA397752026
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6707143G>T , CM000679.2:g.6707143G>T GRCh38
NC_000017.10:g.6610462G>T , CM000679.1:g.6610462G>T GRCh37
NC_000017.9:g.6551186G>T NCBI36
NG_034220.1:g.11279C>A , LRG_1020:g.11279C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.116C>A MANE Select ENSP00000406220.2:p.Ala39Asp
ENST00000293800.10:c.116C>A ENSP00000293800.6:p.Ala39Asp
ENST00000381074.8:c.103-365C>A ENSP00000370464.4:n.103-365C>A
ENST00000433363.6:c.116C>A ENSP00000406220.2:p.Ala39Asp
ENST00000572094.1:c.116C>A ENSP00000461495.1:p.Ala39Asp
ENST00000572352.5:c.103-98C>A ENSP00000461622.1:n.103-98C>A
ENST00000573648.5:c.116C>A ENSP00000459372.1:p.Ala39Asp
ENST00000575230.1:c.116C>A ENSP00000460903.1:p.Ala39Asp
ENST00000576323.1:n.146C>A
NM_001143838.2:c.116C>A NP_001137310.1:p.Ala39Asp
NM_001284509.1:c.116C>A NP_001271438.1:p.Ala39Asp
NM_001284510.1:c.103-365C>A NP_001271439.1:n.103-365C>A
NM_177550.4:c.116C>A , LRG_1020t1:c.116C>A NP_808218.1:p.Ala39Asp
XM_006721504.2:c.103-98C>A XP_006721567.1:n.103-98C>A
XM_011523795.1:c.116C>A XP_011522097.1:p.Ala39Asp
XM_011523795.3:c.116C>A XP_011522097.1:p.Ala39Asp
NM_001143838.3:c.116C>A NP_001137310.1:p.Ala39Asp
NM_001284509.2:c.116C>A NP_001271438.1:p.Ala39Asp
NM_001284510.2:c.103-365C>A NP_001271439.1:n.103-365C>A
NM_177550.5:c.116C>A MANE Select NP_808218.1:p.Ala39Asp