Canonical Allele Identifier: CA2245487620

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695907T= , CM000679.2:g.6695907T=	GRCh38
NC_000017.10:g.6599226T= , CM000679.1:g.6599226T=	GRCh37
NC_000017.9:g.6539950T=	NCBI36
NG_034220.1:g.22515A= , LRG_1020:g.22515A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.874A= MANE Select	ENSP00000406220.2:p.Lys292=
ENST00000293800.10:c.823A=	ENSP00000293800.6:p.Lys275=
ENST00000381074.8:c.745A=	ENSP00000370464.4:p.Lys249=
ENST00000433363.6:c.874A=	ENSP00000406220.2:p.Lys292=
ENST00000572094.1:c.*624A=	ENSP00000461495.1:n.*624A=
ENST00000573648.5:c.874A=	ENSP00000459372.1:p.Lys292=
ENST00000574824.5:n.2007A=
NM_001143838.2:c.874A=	NP_001137310.1:p.Lys292=
NM_001284509.1:c.823A=	NP_001271438.1:p.Lys275=
NM_001284510.1:c.745A=	NP_001271439.1:p.Lys249=
NM_177550.4:c.874A= , LRG_1020t1:c.874A=	NP_808218.1:p.Lys292=
XM_006721504.2:c.763A=	XP_006721567.1:p.Lys255=
XM_011523795.1:c.874A=	XP_011522097.1:p.Lys292=
XM_011523795.3:c.874A=	XP_011522097.1:p.Lys292=
NM_001143838.3:c.874A=	NP_001137310.1:p.Lys292=
NM_001284509.2:c.823A=	NP_001271438.1:p.Lys275=
NM_001284510.2:c.745A=	NP_001271439.1:p.Lys249=
NM_177550.5:c.874A= MANE Select	NP_808218.1:p.Lys292=