Canonical Allele Identifier: CA2245463374
Gene: SLC13A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6706950G= , CM000679.2:g.6706950G= GRCh38
NC_000017.10:g.6610269G= , CM000679.1:g.6610269G= GRCh37
NC_000017.9:g.6550993G= NCBI36
NG_034220.1:g.11472C= , LRG_1020:g.11472C=

Transcript Alleles

HGVS Amino-acid change
ENST00000433363.7:c.231+78C= MANE Select ENSP00000406220.2:n.231+78C=
ENST00000293800.10:c.231+78C= ENSP00000293800.6:n.231+78C=
ENST00000381074.8:c.103-172C= ENSP00000370464.4:n.103-172C=
ENST00000433363.6:c.231+78C= ENSP00000406220.2:n.231+78C=
ENST00000572094.1:c.227+82C= ENSP00000461495.1:n.227+82C=
ENST00000572352.5:c.120+78C= ENSP00000461622.1:n.120+78C=
ENST00000573648.5:c.231+78C= ENSP00000459372.1:n.231+78C=
ENST00000575230.1:c.232-50C= ENSP00000460903.1:n.232-50C=
ENST00000576323.1:n.261+78C=
NM_001143838.2:c.231+78C= NP_001137310.1:n.231+78C=
NM_001284509.1:c.231+78C= NP_001271438.1:n.231+78C=
NM_001284510.1:c.103-172C= NP_001271439.1:n.103-172C=
NM_177550.4:c.231+78C= , LRG_1020t1:c.231+78C= NP_808218.1:n.231+78C=
XM_006721504.2:c.120+78C= XP_006721567.1:n.120+78C=
XM_011523795.1:c.231+78C= XP_011522097.1:n.231+78C=
XM_011523795.3:c.231+78C= XP_011522097.1:n.231+78C=
NM_001143838.3:c.231+78C= NP_001137310.1:n.231+78C=
NM_001284509.2:c.231+78C= NP_001271438.1:n.231+78C=
NM_001284510.2:c.103-172C= NP_001271439.1:n.103-172C=
NM_177550.5:c.231+78C= MANE Select NP_808218.1:n.231+78C=