Canonical Allele Identifier: CA397749983

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6607236G>C (hg19) ; chr17:g.6703917G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703917G>C , CM000679.2:g.6703917G>C	GRCh38
NC_000017.10:g.6607236G>C , CM000679.1:g.6607236G>C	GRCh37
NC_000017.9:g.6547960G>C	NCBI36
NG_034220.1:g.14505C>G , LRG_1020:g.14505C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.508C>G MANE Select	ENSP00000406220.2:p.Leu170Val
ENST00000293800.10:c.457C>G	ENSP00000293800.6:p.Leu153Val
ENST00000381074.8:c.379C>G	ENSP00000370464.4:p.Leu127Val
ENST00000433363.6:c.508C>G	ENSP00000406220.2:p.Leu170Val
ENST00000572094.1:c.*258C>G	ENSP00000461495.1:n.*258C>G
ENST00000572352.5:c.397C>G	ENSP00000461622.1:p.Leu133Val
ENST00000573648.5:c.508C>G	ENSP00000459372.1:p.Leu170Val
ENST00000574824.5:n.1641C>G
ENST00000576323.1:n.538C>G
NM_001143838.2:c.508C>G	NP_001137310.1:p.Leu170Val
NM_001284509.1:c.457C>G	NP_001271438.1:p.Leu153Val
NM_001284510.1:c.379C>G	NP_001271439.1:p.Leu127Val
NM_177550.4:c.508C>G , LRG_1020t1:c.508C>G	NP_808218.1:p.Leu170Val
XM_006721504.2:c.397C>G	XP_006721567.1:p.Leu133Val
XM_011523795.1:c.508C>G	XP_011522097.1:p.Leu170Val
XM_011523795.3:c.508C>G	XP_011522097.1:p.Leu170Val
NM_001143838.3:c.508C>G	NP_001137310.1:p.Leu170Val
NM_001284509.2:c.457C>G	NP_001271438.1:p.Leu153Val
NM_001284510.2:c.379C>G	NP_001271439.1:p.Leu127Val
NM_177550.5:c.508C>G MANE Select	NP_808218.1:p.Leu170Val