Canonical Allele Identifier: CA2366747152

Gene: SLC13A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46613575C= , CM000682.2:g.46613575C=	GRCh38
NC_000020.10:g.45242214C= , CM000682.1:g.45242214C=	GRCh37
NC_000020.9:g.44675621C=	NCBI36
NG_047182.1:g.75911G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279027.9:c.262G= MANE Select	ENSP00000279027.4:p.Asp88=
ENST00000279027.8:c.262G=	ENSP00000279027.4:p.Asp88=
ENST00000290317.9:c.121G=	ENSP00000290317.5:p.Asp41=
ENST00000372121.5:c.121G=	ENSP00000361193.2:p.Asp41=
ENST00000413164.6:c.262G=	ENSP00000415852.2:p.Asp88=
ENST00000417157.2:c.121G=	ENSP00000397955.2:p.Asp41=
ENST00000420568.5:c.151G=	ENSP00000395095.1:p.Asp51=
ENST00000468915.5:c.121G=	ENSP00000417784.1:p.Asp41=
ENST00000472148.5:c.121G=	ENSP00000420177.1:p.Asp41=
ENST00000495082.5:c.121G=	ENSP00000419621.1:p.Asp41=
NM_001011554.2:c.121G=	NP_001011554.1:p.Asp41=
NM_001193339.1:c.262G=	NP_001180268.1:p.Asp88=
NM_001193340.1:c.121G=	NP_001180269.1:p.Asp41=
NM_001193342.1:c.-10-23G=	NP_001180271.1:n.-10-23G=
NM_022829.5:c.262G=	NP_073740.2:p.Asp88=
NM_022829.6:c.262G= MANE Select	NP_073740.2:p.Asp88=
NM_001011554.3:c.121G=	NP_001011554.1:p.Asp41=
NM_001193339.2:c.262G=	NP_001180268.1:p.Asp88=
NM_001193340.2:c.121G=	NP_001180269.1:p.Asp41=
NM_001193342.2:c.-10-23G=	NP_001180271.1:n.-10-23G=