Canonical Allele Identifier: CA409270231
Gene: SLC13A3 HGNC NCBI

Linked Data

dbSNP Id: rs1435204094

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46613641G>C , CM000682.2:g.46613641G>C GRCh38
NC_000020.10:g.45242280G>C , CM000682.1:g.45242280G>C GRCh37
NC_000020.9:g.44675687G>C NCBI36
NG_047182.1:g.75845C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279027.9:c.196C>G MANE Select ENSP00000279027.4:p.Pro66Ala
ENST00000279027.8:c.196C>G ENSP00000279027.4:p.Pro66Ala
ENST00000290317.9:c.55C>G ENSP00000290317.5:p.Pro19Ala
ENST00000372121.5:c.55C>G ENSP00000361193.2:p.Pro19Ala
ENST00000413164.6:c.196C>G ENSP00000415852.2:p.Pro66Ala
ENST00000417157.2:c.55C>G ENSP00000397955.2:p.Pro19Ala
ENST00000420568.5:c.85C>G ENSP00000395095.1:p.Pro29Ala
ENST00000468915.5:c.55C>G ENSP00000417784.1:p.Pro19Ala
ENST00000472148.5:c.55C>G ENSP00000420177.1:p.Pro19Ala
ENST00000495082.5:c.55C>G ENSP00000419621.1:p.Pro19Ala
NM_001011554.2:c.55C>G NP_001011554.1:p.Pro19Ala
NM_001193339.1:c.196C>G NP_001180268.1:p.Pro66Ala
NM_001193340.1:c.55C>G NP_001180269.1:p.Pro19Ala
NM_001193342.1:c.-10-89C>G NP_001180271.1:n.-10-89C>G
NM_022829.5:c.196C>G NP_073740.2:p.Pro66Ala
NM_022829.6:c.196C>G MANE Select NP_073740.2:p.Pro66Ala
NM_001011554.3:c.55C>G NP_001011554.1:p.Pro19Ala
NM_001193339.2:c.196C>G NP_001180268.1:p.Pro66Ala
NM_001193340.2:c.55C>G NP_001180269.1:p.Pro19Ala
NM_001193342.2:c.-10-89C>G NP_001180271.1:n.-10-89C>G