Canonical Allele Identifier: CA409270154

Gene: SLC13A3

Linked Data

• MyVariant Identifiers: chr20:g.45242262A>C (hg19) ; chr20:g.46613623A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46613623A>C , CM000682.2:g.46613623A>C	GRCh38
NC_000020.10:g.45242262A>C , CM000682.1:g.45242262A>C	GRCh37
NC_000020.9:g.44675669A>C	NCBI36
NG_047182.1:g.75863T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279027.9:c.214T>G MANE Select	ENSP00000279027.4:p.Phe72Val
ENST00000279027.8:c.214T>G	ENSP00000279027.4:p.Phe72Val
ENST00000290317.9:c.73T>G	ENSP00000290317.5:p.Phe25Val
ENST00000372121.5:c.73T>G	ENSP00000361193.2:p.Phe25Val
ENST00000413164.6:c.214T>G	ENSP00000415852.2:p.Phe72Val
ENST00000417157.2:c.73T>G	ENSP00000397955.2:p.Phe25Val
ENST00000420568.5:c.103T>G	ENSP00000395095.1:p.Phe35Val
ENST00000468915.5:c.73T>G	ENSP00000417784.1:p.Phe25Val
ENST00000472148.5:c.73T>G	ENSP00000420177.1:p.Phe25Val
ENST00000495082.5:c.73T>G	ENSP00000419621.1:p.Phe25Val
NM_001011554.2:c.73T>G	NP_001011554.1:p.Phe25Val
NM_001193339.1:c.214T>G	NP_001180268.1:p.Phe72Val
NM_001193340.1:c.73T>G	NP_001180269.1:p.Phe25Val
NM_001193342.1:c.-10-71T>G	NP_001180271.1:n.-10-71T>G
NM_022829.5:c.214T>G	NP_073740.2:p.Phe72Val
NM_022829.6:c.214T>G MANE Select	NP_073740.2:p.Phe72Val
NM_001011554.3:c.73T>G	NP_001011554.1:p.Phe25Val
NM_001193339.2:c.214T>G	NP_001180268.1:p.Phe72Val
NM_001193340.2:c.73T>G	NP_001180269.1:p.Phe25Val
NM_001193342.2:c.-10-71T>G	NP_001180271.1:n.-10-71T>G