Canonical Allele Identifier: CA8331570

Gene: SLC13A5

Linked Data

• ClinVar Variation Id: 511849
• ClinVar RCV Id: RCV000950529 ; RCV001718955 ; RCV003905617
• dbSNP Id: rs141287518
• ExAC: 17:6599173 C / T
• gnomAD v2: 17-6599173-C-T
• gnomAD v3: 17-6695854-C-T
• gnomAD v4: 17-6695854-C-T
• MyVariant Identifiers: chr17:g.6599173C>T (hg19) ; chr17:g.6695854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695854C>T , CM000679.2:g.6695854C>T	GRCh38
NC_000017.10:g.6599173C>T , CM000679.1:g.6599173C>T	GRCh37
NC_000017.9:g.6539897C>T	NCBI36
NG_034220.1:g.22568G>A , LRG_1020:g.22568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.927G>A MANE Select	ENSP00000406220.2:p.Leu309=
ENST00000293800.10:c.876G>A	ENSP00000293800.6:p.Leu292=
ENST00000381074.8:c.798G>A	ENSP00000370464.4:p.Leu266=
ENST00000433363.6:c.927G>A	ENSP00000406220.2:p.Leu309=
ENST00000572094.1:c.*677G>A	ENSP00000461495.1:n.*677G>A
ENST00000572727.1:n.36G>A
ENST00000573648.5:c.927G>A	ENSP00000459372.1:p.Leu309=
ENST00000574824.5:n.2060G>A
NM_001143838.2:c.927G>A	NP_001137310.1:p.Leu309=
NM_001284509.1:c.876G>A	NP_001271438.1:p.Leu292=
NM_001284510.1:c.798G>A	NP_001271439.1:p.Leu266=
NM_177550.4:c.927G>A , LRG_1020t1:c.927G>A	NP_808218.1:p.Leu309=
XM_006721504.2:c.816G>A	XP_006721567.1:p.Leu272=
XM_011523795.1:c.927G>A	XP_011522097.1:p.Leu309=
XM_011523795.3:c.927G>A	XP_011522097.1:p.Leu309=
NM_001143838.3:c.927G>A	NP_001137310.1:p.Leu309=
NM_001284509.2:c.876G>A	NP_001271438.1:p.Leu292=
NM_001284510.2:c.798G>A	NP_001271439.1:p.Leu266=
NM_177550.5:c.927G>A MANE Select	NP_808218.1:p.Leu309=