Canonical Allele Identifier: CA397750134

Gene: SLC13A5

Linked Data

• dbSNP Id: rs1177601742
• MyVariant Identifiers: chr17:g.6607307G>A (hg19) ; chr17:g.6703988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703988G>A , CM000679.2:g.6703988G>A	GRCh38
NC_000017.10:g.6607307G>A , CM000679.1:g.6607307G>A	GRCh37
NC_000017.9:g.6548031G>A	NCBI36
NG_034220.1:g.14434C>T , LRG_1020:g.14434C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.437C>T MANE Select	ENSP00000406220.2:p.Ala146Val
ENST00000293800.10:c.386C>T	ENSP00000293800.6:p.Ala129Val
ENST00000381074.8:c.308C>T	ENSP00000370464.4:p.Ala103Val
ENST00000433363.6:c.437C>T	ENSP00000406220.2:p.Ala146Val
ENST00000572094.1:c.*187C>T	ENSP00000461495.1:n.*187C>T
ENST00000572352.5:c.326C>T	ENSP00000461622.1:p.Ala109Val
ENST00000573648.5:c.437C>T	ENSP00000459372.1:p.Ala146Val
ENST00000574824.5:n.1570C>T
ENST00000576323.1:n.467C>T
NM_001143838.2:c.437C>T	NP_001137310.1:p.Ala146Val
NM_001284509.1:c.386C>T	NP_001271438.1:p.Ala129Val
NM_001284510.1:c.308C>T	NP_001271439.1:p.Ala103Val
NM_177550.4:c.437C>T , LRG_1020t1:c.437C>T	NP_808218.1:p.Ala146Val
XM_006721504.2:c.326C>T	XP_006721567.1:p.Ala109Val
XM_011523795.1:c.437C>T	XP_011522097.1:p.Ala146Val
XM_011523795.3:c.437C>T	XP_011522097.1:p.Ala146Val
NM_001143838.3:c.437C>T	NP_001137310.1:p.Ala146Val
NM_001284509.2:c.386C>T	NP_001271438.1:p.Ala129Val
NM_001284510.2:c.308C>T	NP_001271439.1:p.Ala103Val
NM_177550.5:c.437C>T MANE Select	NP_808218.1:p.Ala146Val