Canonical Allele Identifier: CA2245460176

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703939T= , CM000679.2:g.6703939T=	GRCh38
NC_000017.10:g.6607258T= , CM000679.1:g.6607258T=	GRCh37
NC_000017.9:g.6547982T=	NCBI36
NG_034220.1:g.14483A= , LRG_1020:g.14483A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.486A= MANE Select	ENSP00000406220.2:p.Thr162=
ENST00000293800.10:c.435A=	ENSP00000293800.6:p.Thr145=
ENST00000381074.8:c.357A=	ENSP00000370464.4:p.Thr119=
ENST00000433363.6:c.486A=	ENSP00000406220.2:p.Thr162=
ENST00000572094.1:c.*236A=	ENSP00000461495.1:n.*236A=
ENST00000572352.5:c.375A=	ENSP00000461622.1:p.Thr125=
ENST00000573648.5:c.486A=	ENSP00000459372.1:p.Thr162=
ENST00000574824.5:n.1619A=
ENST00000576323.1:n.516A=
NM_001143838.2:c.486A=	NP_001137310.1:p.Thr162=
NM_001284509.1:c.435A=	NP_001271438.1:p.Thr145=
NM_001284510.1:c.357A=	NP_001271439.1:p.Thr119=
NM_177550.4:c.486A= , LRG_1020t1:c.486A=	NP_808218.1:p.Thr162=
XM_006721504.2:c.375A=	XP_006721567.1:p.Thr125=
XM_011523795.1:c.486A=	XP_011522097.1:p.Thr162=
XM_011523795.3:c.486A=	XP_011522097.1:p.Thr162=
NM_001143838.3:c.486A=	NP_001137310.1:p.Thr162=
NM_001284509.2:c.435A=	NP_001271438.1:p.Thr145=
NM_001284510.2:c.357A=	NP_001271439.1:p.Thr119=
NM_177550.5:c.486A= MANE Select	NP_808218.1:p.Thr162=