Canonical Allele Identifier: CA497596351

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6599233T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695914T>C , CM000679.2:g.6695914T>C	GRCh38
NC_000017.10:g.6599233T>C , CM000679.1:g.6599233T>C	GRCh37
NC_000017.9:g.6539957T>C	NCBI36
NG_034220.1:g.22508A>G , LRG_1020:g.22508A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.867A>G MANE Select	ENSP00000406220.2:p.Leu289=
ENST00000293800.10:c.816A>G	ENSP00000293800.6:p.Leu272=
ENST00000381074.8:c.738A>G	ENSP00000370464.4:p.Leu246=
ENST00000433363.6:c.867A>G	ENSP00000406220.2:p.Leu289=
ENST00000572094.1:c.*617A>G	ENSP00000461495.1:n.*617A>G
ENST00000573648.5:c.867A>G	ENSP00000459372.1:p.Leu289=
ENST00000574824.5:n.2000A>G
NM_001143838.2:c.867A>G	NP_001137310.1:p.Leu289=
NM_001284509.1:c.816A>G	NP_001271438.1:p.Leu272=
NM_001284510.1:c.738A>G	NP_001271439.1:p.Leu246=
NM_177550.4:c.867A>G , LRG_1020t1:c.867A>G	NP_808218.1:p.Leu289=
XM_006721504.2:c.756A>G	XP_006721567.1:p.Leu252=
XM_011523795.1:c.867A>G	XP_011522097.1:p.Leu289=
XM_011523795.3:c.867A>G	XP_011522097.1:p.Leu289=
NM_001143838.3:c.867A>G	NP_001137310.1:p.Leu289=
NM_001284509.2:c.816A>G	NP_001271438.1:p.Leu272=
NM_001284510.2:c.738A>G	NP_001271439.1:p.Leu246=
NM_177550.5:c.867A>G MANE Select	NP_808218.1:p.Leu289=