Canonical Allele Identifier: CA2245487560

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695766G= , CM000679.2:g.6695766G=	GRCh38
NC_000017.10:g.6599085G= , CM000679.1:g.6599085G=	GRCh37
NC_000017.9:g.6539809G=	NCBI36
NG_034220.1:g.22656C= , LRG_1020:g.22656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1015C= MANE Select	ENSP00000406220.2:p.Pro339=
ENST00000293800.10:c.964C=	ENSP00000293800.6:p.Pro322=
ENST00000381074.8:c.886C=	ENSP00000370464.4:p.Pro296=
ENST00000433363.6:c.1015C=	ENSP00000406220.2:p.Pro339=
ENST00000572727.1:n.124C=
ENST00000573648.5:c.1015C=	ENSP00000459372.1:p.Pro339=
ENST00000574824.5:n.2148C=
NM_001143838.2:c.1015C=	NP_001137310.1:p.Pro339=
NM_001284509.1:c.964C=	NP_001271438.1:p.Pro322=
NM_001284510.1:c.886C=	NP_001271439.1:p.Pro296=
NM_177550.4:c.1015C= , LRG_1020t1:c.1015C=	NP_808218.1:p.Pro339=
XM_006721504.2:c.904C=	XP_006721567.1:p.Pro302=
XM_011523795.1:c.1015C=	XP_011522097.1:p.Pro339=
XM_011523795.3:c.1015C=	XP_011522097.1:p.Pro339=
NM_001143838.3:c.1015C=	NP_001137310.1:p.Pro339=
NM_001284509.2:c.964C=	NP_001271438.1:p.Pro322=
NM_001284510.2:c.886C=	NP_001271439.1:p.Pro296=
NM_177550.5:c.1015C= MANE Select	NP_808218.1:p.Pro339=