Canonical Allele Identifier: CA2245460237

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703971C= , CM000679.2:g.6703971C=	GRCh38
NC_000017.10:g.6607290C= , CM000679.1:g.6607290C=	GRCh37
NC_000017.9:g.6548014C=	NCBI36
NG_034220.1:g.14451G= , LRG_1020:g.14451G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.454G= MANE Select	ENSP00000406220.2:p.Val152=
ENST00000293800.10:c.403G=	ENSP00000293800.6:p.Val135=
ENST00000381074.8:c.325G=	ENSP00000370464.4:p.Val109=
ENST00000433363.6:c.454G=	ENSP00000406220.2:p.Val152=
ENST00000572094.1:c.*204G=	ENSP00000461495.1:n.*204G=
ENST00000572352.5:c.343G=	ENSP00000461622.1:p.Val115=
ENST00000573648.5:c.454G=	ENSP00000459372.1:p.Val152=
ENST00000574824.5:n.1587G=
ENST00000576323.1:n.484G=
NM_001143838.2:c.454G=	NP_001137310.1:p.Val152=
NM_001284509.1:c.403G=	NP_001271438.1:p.Val135=
NM_001284510.1:c.325G=	NP_001271439.1:p.Val109=
NM_177550.4:c.454G= , LRG_1020t1:c.454G=	NP_808218.1:p.Val152=
XM_006721504.2:c.343G=	XP_006721567.1:p.Val115=
XM_011523795.1:c.454G=	XP_011522097.1:p.Val152=
XM_011523795.3:c.454G=	XP_011522097.1:p.Val152=
NM_001143838.3:c.454G=	NP_001137310.1:p.Val152=
NM_001284509.2:c.403G=	NP_001271438.1:p.Val135=
NM_001284510.2:c.325G=	NP_001271439.1:p.Val109=
NM_177550.5:c.454G= MANE Select	NP_808218.1:p.Val152=