Canonical Allele Identifier: CA8331575

Gene: SLC13A5

Linked Data

• dbSNP Id: rs749077002
• ExAC: 17:6599217 C / G
• gnomAD v2: 17-6599217-C-G
• gnomAD v3: 17-6695898-C-G
• gnomAD v4: 17-6695898-C-G
• MyVariant Identifiers: chr17:g.6599217C>G (hg19) ; chr17:g.6695898C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695898C>G , CM000679.2:g.6695898C>G	GRCh38
NC_000017.10:g.6599217C>G , CM000679.1:g.6599217C>G	GRCh37
NC_000017.9:g.6539941C>G	NCBI36
NG_034220.1:g.22524G>C , LRG_1020:g.22524G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.883G>C MANE Select	ENSP00000406220.2:p.Glu295Gln
ENST00000293800.10:c.832G>C	ENSP00000293800.6:p.Glu278Gln
ENST00000381074.8:c.754G>C	ENSP00000370464.4:p.Glu252Gln
ENST00000433363.6:c.883G>C	ENSP00000406220.2:p.Glu295Gln
ENST00000572094.1:c.*633G>C	ENSP00000461495.1:n.*633G>C
ENST00000573648.5:c.883G>C	ENSP00000459372.1:p.Glu295Gln
ENST00000574824.5:n.2016G>C
NM_001143838.2:c.883G>C	NP_001137310.1:p.Glu295Gln
NM_001284509.1:c.832G>C	NP_001271438.1:p.Glu278Gln
NM_001284510.1:c.754G>C	NP_001271439.1:p.Glu252Gln
NM_177550.4:c.883G>C , LRG_1020t1:c.883G>C	NP_808218.1:p.Glu295Gln
XM_006721504.2:c.772G>C	XP_006721567.1:p.Glu258Gln
XM_011523795.1:c.883G>C	XP_011522097.1:p.Glu295Gln
XM_011523795.3:c.883G>C	XP_011522097.1:p.Glu295Gln
NM_001143838.3:c.883G>C	NP_001137310.1:p.Glu295Gln
NM_001284509.2:c.832G>C	NP_001271438.1:p.Glu278Gln
NM_001284510.2:c.754G>C	NP_001271439.1:p.Glu252Gln
NM_177550.5:c.883G>C MANE Select	NP_808218.1:p.Glu295Gln