Canonical Allele Identifier: CA497596657

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6607375C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6704056C>A , CM000679.2:g.6704056C>A	GRCh38
NC_000017.10:g.6607375C>A , CM000679.1:g.6607375C>A	GRCh37
NC_000017.9:g.6548099C>A	NCBI36
NG_034220.1:g.14366G>T , LRG_1020:g.14366G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.369G>T MANE Select	ENSP00000406220.2:p.Arg123=
ENST00000293800.10:c.369-51G>T	ENSP00000293800.6:n.369-51G>T
ENST00000381074.8:c.240G>T	ENSP00000370464.4:p.Arg80=
ENST00000433363.6:c.369G>T	ENSP00000406220.2:p.Arg123=
ENST00000572094.1:c.*119G>T	ENSP00000461495.1:n.*119G>T
ENST00000572352.5:c.258G>T	ENSP00000461622.1:p.Arg86=
ENST00000573648.5:c.369G>T	ENSP00000459372.1:p.Arg123=
ENST00000574824.5:n.1502G>T
ENST00000575230.1:c.*215G>T	ENSP00000460903.1:n.*215G>T
ENST00000576323.1:n.399G>T
NM_001143838.2:c.369G>T	NP_001137310.1:p.Arg123=
NM_001284509.1:c.369-51G>T	NP_001271438.1:n.369-51G>T
NM_001284510.1:c.240G>T	NP_001271439.1:p.Arg80=
NM_177550.4:c.369G>T , LRG_1020t1:c.369G>T	NP_808218.1:p.Arg123=
XM_006721504.2:c.258G>T	XP_006721567.1:p.Arg86=
XM_011523795.1:c.369G>T	XP_011522097.1:p.Arg123=
XM_011523795.3:c.369G>T	XP_011522097.1:p.Arg123=
NM_001143838.3:c.369G>T	NP_001137310.1:p.Arg123=
NM_001284509.2:c.369-51G>T	NP_001271438.1:n.369-51G>T
NM_001284510.2:c.240G>T	NP_001271439.1:p.Arg80=
NM_177550.5:c.369G>T MANE Select	NP_808218.1:p.Arg123=