Canonical Allele Identifier: CA2245458987

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703031C= , CM000679.2:g.6703031C=	GRCh38
NC_000017.10:g.6606350C= , CM000679.1:g.6606350C=	GRCh37
NC_000017.9:g.6547074C=	NCBI36
NG_034220.1:g.15391G= , LRG_1020:g.15391G=

Transcript Alleles

HGVS	Amino-acid Change
NM_177550.5:c.655G= MANE Select	NP_808218.1:p.Gly219=
ENST00000433363.7:c.655G= MANE Select	ENSP00000406220.2:p.Gly219=
NM_001143838.2:c.655G=	NP_001137310.1:p.Gly219=
NM_001143838.3:c.655G=	NP_001137310.1:p.Gly219=
NM_001284509.1:c.604G=	NP_001271438.1:p.Gly202=
NM_001284509.2:c.604G=	NP_001271438.1:p.Gly202=
NM_001284510.1:c.526G=	NP_001271439.1:p.Gly176=
NM_001284510.2:c.526G=	NP_001271439.1:p.Gly176=
NM_177550.4:c.655G= , LRG_1020t1:c.655G=	NP_808218.1:p.Gly219=
ENST00000293800.10:c.604G=	ENSP00000293800.6:p.Gly202=
ENST00000381074.8:c.526G=	ENSP00000370464.4:p.Gly176=
ENST00000433363.6:c.655G=	ENSP00000406220.2:p.Gly219=
ENST00000572094.1:c.*405G=	ENSP00000461495.1:n.*405G=
ENST00000573648.5:c.655G=	ENSP00000459372.1:p.Gly219=
ENST00000574824.5:n.1788G=
XM_006721504.2:c.544G=	XP_006721567.1:p.Gly182=
XM_011523795.1:c.655G=	XP_011522097.1:p.Gly219=
XM_011523795.3:c.655G=	XP_011522097.1:p.Gly219=