Canonical Allele Identifier: CA2245458704
Gene: SLC13A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6702909C= , CM000679.2:g.6702909C= GRCh38
NC_000017.10:g.6606228C= , CM000679.1:g.6606228C= GRCh37
NC_000017.9:g.6546952C= NCBI36
NG_034220.1:g.15513G= , LRG_1020:g.15513G=

Transcript Alleles

HGVS Amino-acid change
ENST00000433363.7:c.716+61G= MANE Select ENSP00000406220.2:n.716+61G=
ENST00000293800.10:c.665+61G= ENSP00000293800.6:n.665+61G=
ENST00000381074.8:c.587+61G= ENSP00000370464.4:n.587+61G=
ENST00000433363.6:c.716+61G= ENSP00000406220.2:n.716+61G=
ENST00000572094.1:c.*466+61G= ENSP00000461495.1:n.*466+61G=
ENST00000573648.5:c.716+61G= ENSP00000459372.1:n.716+61G=
ENST00000574824.5:n.1849+61G=
NM_001143838.2:c.716+61G= NP_001137310.1:n.716+61G=
NM_001284509.1:c.665+61G= NP_001271438.1:n.665+61G=
NM_001284510.1:c.587+61G= NP_001271439.1:n.587+61G=
NM_177550.4:c.716+61G= , LRG_1020t1:c.716+61G= NP_808218.1:n.716+61G=
XM_006721504.2:c.605+61G= XP_006721567.1:n.605+61G=
XM_011523795.1:c.716+61G= XP_011522097.1:n.716+61G=
XM_011523795.3:c.716+61G= XP_011522097.1:n.716+61G=
NM_001143838.3:c.716+61G= NP_001137310.1:n.716+61G=
NM_001284509.2:c.665+61G= NP_001271438.1:n.665+61G=
NM_001284510.2:c.587+61G= NP_001271439.1:n.587+61G=
NM_177550.5:c.716+61G= MANE Select NP_808218.1:n.716+61G=