Canonical Allele Identifier: CA397750137
Gene: SLC13A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703989C>A , CM000679.2:g.6703989C>A GRCh38
NC_000017.10:g.6607308C>A , CM000679.1:g.6607308C>A GRCh37
NC_000017.9:g.6548032C>A NCBI36
NG_034220.1:g.14433G>T , LRG_1020:g.14433G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433363.7:c.436G>T MANE Select ENSP00000406220.2:p.Ala146Ser
ENST00000293800.10:c.385G>T ENSP00000293800.6:p.Ala129Ser
ENST00000381074.8:c.307G>T ENSP00000370464.4:p.Ala103Ser
ENST00000433363.6:c.436G>T ENSP00000406220.2:p.Ala146Ser
ENST00000572094.1:c.*186G>T ENSP00000461495.1:n.*186G>T
ENST00000572352.5:c.325G>T ENSP00000461622.1:p.Ala109Ser
ENST00000573648.5:c.436G>T ENSP00000459372.1:p.Ala146Ser
ENST00000574824.5:n.1569G>T
ENST00000576323.1:n.466G>T
NM_001143838.2:c.436G>T NP_001137310.1:p.Ala146Ser
NM_001284509.1:c.385G>T NP_001271438.1:p.Ala129Ser
NM_001284510.1:c.307G>T NP_001271439.1:p.Ala103Ser
NM_177550.4:c.436G>T , LRG_1020t1:c.436G>T NP_808218.1:p.Ala146Ser
XM_006721504.2:c.325G>T XP_006721567.1:p.Ala109Ser
XM_011523795.1:c.436G>T XP_011522097.1:p.Ala146Ser
XM_011523795.3:c.436G>T XP_011522097.1:p.Ala146Ser
NM_001143838.3:c.436G>T NP_001137310.1:p.Ala146Ser
NM_001284509.2:c.385G>T NP_001271438.1:p.Ala129Ser
NM_001284510.2:c.307G>T NP_001271439.1:p.Ala103Ser
NM_177550.5:c.436G>T MANE Select NP_808218.1:p.Ala146Ser