Canonical Allele Identifier: CA2245460109

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703909C= , CM000679.2:g.6703909C=	GRCh38
NC_000017.10:g.6607228C= , CM000679.1:g.6607228C=	GRCh37
NC_000017.9:g.6547952C=	NCBI36
NG_034220.1:g.14513G= , LRG_1020:g.14513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.516G= MANE Select	ENSP00000406220.2:p.Leu172=
ENST00000293800.10:c.465G=	ENSP00000293800.6:p.Leu155=
ENST00000381074.8:c.387G=	ENSP00000370464.4:p.Leu129=
ENST00000433363.6:c.516G=	ENSP00000406220.2:p.Leu172=
ENST00000572094.1:c.*266G=	ENSP00000461495.1:n.*266G=
ENST00000572352.5:c.405G=	ENSP00000461622.1:p.Leu135=
ENST00000573648.5:c.516G=	ENSP00000459372.1:p.Leu172=
ENST00000574824.5:n.1649G=
ENST00000576323.1:n.546G=
NM_001143838.2:c.516G=	NP_001137310.1:p.Leu172=
NM_001284509.1:c.465G=	NP_001271438.1:p.Leu155=
NM_001284510.1:c.387G=	NP_001271439.1:p.Leu129=
NM_177550.4:c.516G= , LRG_1020t1:c.516G=	NP_808218.1:p.Leu172=
XM_006721504.2:c.405G=	XP_006721567.1:p.Leu135=
XM_011523795.1:c.516G=	XP_011522097.1:p.Leu172=
XM_011523795.3:c.516G=	XP_011522097.1:p.Leu172=
NM_001143838.3:c.516G=	NP_001137310.1:p.Leu172=
NM_001284509.2:c.465G=	NP_001271438.1:p.Leu155=
NM_001284510.2:c.387G=	NP_001271439.1:p.Leu129=
NM_177550.5:c.516G= MANE Select	NP_808218.1:p.Leu172=