Canonical Allele Identifier: CA2245458966

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703023G= , CM000679.2:g.6703023G=	GRCh38
NC_000017.10:g.6606342G= , CM000679.1:g.6606342G=	GRCh37
NC_000017.9:g.6547066G=	NCBI36
NG_034220.1:g.15399C= , LRG_1020:g.15399C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.663C= MANE Select	ENSP00000406220.2:p.Thr221=
ENST00000293800.10:c.612C=	ENSP00000293800.6:p.Thr204=
ENST00000381074.8:c.534C=	ENSP00000370464.4:p.Thr178=
ENST00000433363.6:c.663C=	ENSP00000406220.2:p.Thr221=
ENST00000572094.1:c.*413C=	ENSP00000461495.1:n.*413C=
ENST00000573648.5:c.663C=	ENSP00000459372.1:p.Thr221=
ENST00000574824.5:n.1796C=
NM_001143838.2:c.663C=	NP_001137310.1:p.Thr221=
NM_001284509.1:c.612C=	NP_001271438.1:p.Thr204=
NM_001284510.1:c.534C=	NP_001271439.1:p.Thr178=
NM_177550.4:c.663C= , LRG_1020t1:c.663C=	NP_808218.1:p.Thr221=
XM_006721504.2:c.552C=	XP_006721567.1:p.Thr184=
XM_011523795.1:c.663C=	XP_011522097.1:p.Thr221=
XM_011523795.3:c.663C=	XP_011522097.1:p.Thr221=
NM_001143838.3:c.663C=	NP_001137310.1:p.Thr221=
NM_001284509.2:c.612C=	NP_001271438.1:p.Thr204=
NM_001284510.2:c.534C=	NP_001271439.1:p.Thr178=
NM_177550.5:c.663C= MANE Select	NP_808218.1:p.Thr221=