Canonical Allele Identifier: CA8331706

Gene: SLC13A5

Linked Data

• ClinVar Variation Id: 1588311
• ClinVar RCV Id: RCV002096008
• dbSNP Id: rs367895721
• ExAC: 17:6607273 C / T
• gnomAD v2: 17-6607273-C-T
• gnomAD v3: 17-6703954-C-T
• gnomAD v4: 17-6703954-C-T
• MyVariant Identifiers: chr17:g.6607273C>T (hg19) ; chr17:g.6703954C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703954C>T , CM000679.2:g.6703954C>T	GRCh38
NC_000017.10:g.6607273C>T , CM000679.1:g.6607273C>T	GRCh37
NC_000017.9:g.6547997C>T	NCBI36
NG_034220.1:g.14468G>A , LRG_1020:g.14468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.471G>A MANE Select	ENSP00000406220.2:p.Gln157=
ENST00000293800.10:c.420G>A	ENSP00000293800.6:p.Gln140=
ENST00000381074.8:c.342G>A	ENSP00000370464.4:p.Gln114=
ENST00000433363.6:c.471G>A	ENSP00000406220.2:p.Gln157=
ENST00000572094.1:c.*221G>A	ENSP00000461495.1:n.*221G>A
ENST00000572352.5:c.360G>A	ENSP00000461622.1:p.Gln120=
ENST00000573648.5:c.471G>A	ENSP00000459372.1:p.Gln157=
ENST00000574824.5:n.1604G>A
ENST00000576323.1:n.501G>A
NM_001143838.2:c.471G>A	NP_001137310.1:p.Gln157=
NM_001284509.1:c.420G>A	NP_001271438.1:p.Gln140=
NM_001284510.1:c.342G>A	NP_001271439.1:p.Gln114=
NM_177550.4:c.471G>A , LRG_1020t1:c.471G>A	NP_808218.1:p.Gln157=
XM_006721504.2:c.360G>A	XP_006721567.1:p.Gln120=
XM_011523795.1:c.471G>A	XP_011522097.1:p.Gln157=
XM_011523795.3:c.471G>A	XP_011522097.1:p.Gln157=
NM_001143838.3:c.471G>A	NP_001137310.1:p.Gln157=
NM_001284509.2:c.420G>A	NP_001271438.1:p.Gln140=
NM_001284510.2:c.342G>A	NP_001271439.1:p.Gln114=
NM_177550.5:c.471G>A MANE Select	NP_808218.1:p.Gln157=