Canonical Allele Identifier: CA744886483

Gene: SLC13A3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46659814G>T , CM000682.2:g.46659814G>T	GRCh38
NC_000020.10:g.45288453G>T , CM000682.1:g.45288453G>T	GRCh37
NC_000020.9:g.44721860G>T	NCBI36
NG_047182.1:g.29672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290317.9:c.-31+10229C>A	ENSP00000290317.5:n.-31+10229C>A
ENST00000372121.5:c.-31+24582C>A	ENSP00000361193.2:n.-31+24582C>A
ENST00000417157.2:c.-31+10229C>A	ENSP00000397955.2:n.-31+10229C>A
ENST00000468915.5:c.-31+10229C>A	ENSP00000417784.1:n.-31+10229C>A
ENST00000472148.5:c.-31+10229C>A	ENSP00000420177.1:n.-31+10229C>A
NM_001011554.2:c.-31+10229C>A	NP_001011554.1:n.-31+10229C>A
NM_001193340.1:c.-31+10229C>A	NP_001180269.1:n.-31+10229C>A
NM_001011554.3:c.-31+10229C>A	NP_001011554.1:n.-31+10229C>A
NM_001193340.2:c.-31+10229C>A	NP_001180269.1:n.-31+10229C>A