Canonical Allele Identifier: CA2245460205

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703954C= , CM000679.2:g.6703954C=	GRCh38
NC_000017.10:g.6607273C= , CM000679.1:g.6607273C=	GRCh37
NC_000017.9:g.6547997C=	NCBI36
NG_034220.1:g.14468G= , LRG_1020:g.14468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.471G= MANE Select	ENSP00000406220.2:p.Gln157=
ENST00000293800.10:c.420G=	ENSP00000293800.6:p.Gln140=
ENST00000381074.8:c.342G=	ENSP00000370464.4:p.Gln114=
ENST00000433363.6:c.471G=	ENSP00000406220.2:p.Gln157=
ENST00000572094.1:c.*221G=	ENSP00000461495.1:n.*221G=
ENST00000572352.5:c.360G=	ENSP00000461622.1:p.Gln120=
ENST00000573648.5:c.471G=	ENSP00000459372.1:p.Gln157=
ENST00000574824.5:n.1604G=
ENST00000576323.1:n.501G=
NM_001143838.2:c.471G=	NP_001137310.1:p.Gln157=
NM_001284509.1:c.420G=	NP_001271438.1:p.Gln140=
NM_001284510.1:c.342G=	NP_001271439.1:p.Gln114=
NM_177550.4:c.471G= , LRG_1020t1:c.471G=	NP_808218.1:p.Gln157=
XM_006721504.2:c.360G=	XP_006721567.1:p.Gln120=
XM_011523795.1:c.471G=	XP_011522097.1:p.Gln157=
XM_011523795.3:c.471G=	XP_011522097.1:p.Gln157=
NM_001143838.3:c.471G=	NP_001137310.1:p.Gln157=
NM_001284509.2:c.420G=	NP_001271438.1:p.Gln140=
NM_001284510.2:c.342G=	NP_001271439.1:p.Gln114=
NM_177550.5:c.471G= MANE Select	NP_808218.1:p.Gln157=