Canonical Allele Identifier: CA8331717

Gene: SLC13A5

Linked Data

• ClinVar Variation Id: 2176492
• ClinVar RCV Id: RCV002602635
• dbSNP Id: rs560631853
• ExAC: 17:6607309 C / T
• gnomAD v2: 17-6607309-C-T
• gnomAD v3: 17-6703990-C-T
• gnomAD v4: 17-6703990-C-T
• MyVariant Identifiers: chr17:g.6607309C>T (hg19) ; chr17:g.6703990C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703990C>T , CM000679.2:g.6703990C>T	GRCh38
NC_000017.10:g.6607309C>T , CM000679.1:g.6607309C>T	GRCh37
NC_000017.9:g.6548033C>T	NCBI36
NG_034220.1:g.14432G>A , LRG_1020:g.14432G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.435G>A MANE Select	ENSP00000406220.2:p.Thr145=
ENST00000293800.10:c.384G>A	ENSP00000293800.6:p.Thr128=
ENST00000381074.8:c.306G>A	ENSP00000370464.4:p.Thr102=
ENST00000433363.6:c.435G>A	ENSP00000406220.2:p.Thr145=
ENST00000572094.1:c.*185G>A	ENSP00000461495.1:n.*185G>A
ENST00000572352.5:c.324G>A	ENSP00000461622.1:p.Thr108=
ENST00000573648.5:c.435G>A	ENSP00000459372.1:p.Thr145=
ENST00000574824.5:n.1568G>A
ENST00000576323.1:n.465G>A
NM_001143838.2:c.435G>A	NP_001137310.1:p.Thr145=
NM_001284509.1:c.384G>A	NP_001271438.1:p.Thr128=
NM_001284510.1:c.306G>A	NP_001271439.1:p.Thr102=
NM_177550.4:c.435G>A , LRG_1020t1:c.435G>A	NP_808218.1:p.Thr145=
XM_006721504.2:c.324G>A	XP_006721567.1:p.Thr108=
XM_011523795.1:c.435G>A	XP_011522097.1:p.Thr145=
XM_011523795.3:c.435G>A	XP_011522097.1:p.Thr145=
NM_001143838.3:c.435G>A	NP_001137310.1:p.Thr145=
NM_001284509.2:c.384G>A	NP_001271438.1:p.Thr128=
NM_001284510.2:c.306G>A	NP_001271439.1:p.Thr102=
NM_177550.5:c.435G>A MANE Select	NP_808218.1:p.Thr145=