Canonical Allele Identifier: CA409269753

Gene: SLC13A3

Linked Data

• gnomAD v4: 20-46613551-C-A
• MyVariant Identifiers: chr20:g.45242190C>A (hg19) ; chr20:g.46613551C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46613551C>A , CM000682.2:g.46613551C>A	GRCh38
NC_000020.10:g.45242190C>A , CM000682.1:g.45242190C>A	GRCh37
NC_000020.9:g.44675597C>A	NCBI36
NG_047182.1:g.75935G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279027.9:c.286G>T MANE Select	ENSP00000279027.4:p.Gly96Trp
ENST00000279027.8:c.286G>T	ENSP00000279027.4:p.Gly96Trp
ENST00000290317.9:c.145G>T	ENSP00000290317.5:p.Gly49Trp
ENST00000372121.5:c.145G>T	ENSP00000361193.2:p.Gly49Trp
ENST00000413164.6:c.286G>T	ENSP00000415852.2:p.Gly96Trp
ENST00000417157.2:c.145G>T	ENSP00000397955.2:p.Gly49Trp
ENST00000420568.5:c.175G>T	ENSP00000395095.1:p.Gly59Trp
ENST00000468915.5:c.145G>T	ENSP00000417784.1:p.Gly49Trp
ENST00000472148.5:c.145G>T	ENSP00000420177.1:p.Gly49Trp
ENST00000495082.5:c.145G>T	ENSP00000419621.1:p.Gly49Trp
NM_001011554.2:c.145G>T	NP_001011554.1:p.Gly49Trp
NM_001193339.1:c.286G>T	NP_001180268.1:p.Gly96Trp
NM_001193340.1:c.145G>T	NP_001180269.1:p.Gly49Trp
NM_001193342.1:c.-9G>T	NP_001180271.1:n.-9G>T
NM_022829.5:c.286G>T	NP_073740.2:p.Gly96Trp
NM_022829.6:c.286G>T MANE Select	NP_073740.2:p.Gly96Trp
NM_001011554.3:c.145G>T	NP_001011554.1:p.Gly49Trp
NM_001193339.2:c.286G>T	NP_001180268.1:p.Gly96Trp
NM_001193340.2:c.145G>T	NP_001180269.1:p.Gly49Trp
NM_001193342.2:c.-9G>T	NP_001180271.1:n.-9G>T