Canonical Allele Identifier: CA2245487555

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695753G= , CM000679.2:g.6695753G=	GRCh38
NC_000017.10:g.6599072G= , CM000679.1:g.6599072G=	GRCh37
NC_000017.9:g.6539796G=	NCBI36
NG_034220.1:g.22669C= , LRG_1020:g.22669C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1028C= MANE Select	ENSP00000406220.2:p.Thr343=
ENST00000293800.10:c.977C=	ENSP00000293800.6:p.Thr326=
ENST00000381074.8:c.899C=	ENSP00000370464.4:p.Thr300=
ENST00000433363.6:c.1028C=	ENSP00000406220.2:p.Thr343=
ENST00000572727.1:n.137C=
ENST00000573648.5:c.1028C=	ENSP00000459372.1:p.Thr343=
ENST00000574824.5:n.2161C=
NM_001143838.2:c.1028C=	NP_001137310.1:p.Thr343=
NM_001284509.1:c.977C=	NP_001271438.1:p.Thr326=
NM_001284510.1:c.899C=	NP_001271439.1:p.Thr300=
NM_177550.4:c.1028C= , LRG_1020t1:c.1028C=	NP_808218.1:p.Thr343=
XM_006721504.2:c.917C=	XP_006721567.1:p.Thr306=
XM_011523795.1:c.1028C=	XP_011522097.1:p.Thr343=
XM_011523795.3:c.1028C=	XP_011522097.1:p.Thr343=
NM_001143838.3:c.1028C=	NP_001137310.1:p.Thr343=
NM_001284509.2:c.977C=	NP_001271438.1:p.Thr326=
NM_001284510.2:c.899C=	NP_001271439.1:p.Thr300=
NM_177550.5:c.1028C= MANE Select	NP_808218.1:p.Thr343=