Canonical Allele Identifier: CA397744617

Gene: SLC13A5

Linked Data

• gnomAD v4: 17-6695866-C-G
• MyVariant Identifiers: chr17:g.6599185C>G (hg19) ; chr17:g.6695866C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695866C>G , CM000679.2:g.6695866C>G	GRCh38
NC_000017.10:g.6599185C>G , CM000679.1:g.6599185C>G	GRCh37
NC_000017.9:g.6539909C>G	NCBI36
NG_034220.1:g.22556G>C , LRG_1020:g.22556G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.915G>C MANE Select	ENSP00000406220.2:p.Glu305Asp
ENST00000293800.10:c.864G>C	ENSP00000293800.6:p.Glu288Asp
ENST00000381074.8:c.786G>C	ENSP00000370464.4:p.Glu262Asp
ENST00000433363.6:c.915G>C	ENSP00000406220.2:p.Glu305Asp
ENST00000572094.1:c.*665G>C	ENSP00000461495.1:n.*665G>C
ENST00000572727.1:n.24G>C
ENST00000573648.5:c.915G>C	ENSP00000459372.1:p.Glu305Asp
ENST00000574824.5:n.2048G>C
NM_001143838.2:c.915G>C	NP_001137310.1:p.Glu305Asp
NM_001284509.1:c.864G>C	NP_001271438.1:p.Glu288Asp
NM_001284510.1:c.786G>C	NP_001271439.1:p.Glu262Asp
NM_177550.4:c.915G>C , LRG_1020t1:c.915G>C	NP_808218.1:p.Glu305Asp
XM_006721504.2:c.804G>C	XP_006721567.1:p.Glu268Asp
XM_011523795.1:c.915G>C	XP_011522097.1:p.Glu305Asp
XM_011523795.3:c.915G>C	XP_011522097.1:p.Glu305Asp
NM_001143838.3:c.915G>C	NP_001137310.1:p.Glu305Asp
NM_001284509.2:c.864G>C	NP_001271438.1:p.Glu288Asp
NM_001284510.2:c.786G>C	NP_001271439.1:p.Glu262Asp
NM_177550.5:c.915G>C MANE Select	NP_808218.1:p.Glu305Asp