Canonical Allele Identifier: CA624676818

Gene: SLC13A5

Linked Data

• dbSNP Id: rs1267016196
• gnomAD v2: 17-6607404-A-G
• gnomAD v4: 17-6704085-A-G
• MyVariant Identifiers: chr17:g.6607404A>G (hg19) ; chr17:g.6704085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6704085A>G , CM000679.2:g.6704085A>G	GRCh38
NC_000017.10:g.6607404A>G , CM000679.1:g.6607404A>G	GRCh37
NC_000017.9:g.6548128A>G	NCBI36
NG_034220.1:g.14337T>C , LRG_1020:g.14337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.369-29T>C MANE Select	ENSP00000406220.2:n.369-29T>C
ENST00000293800.10:c.369-80T>C	ENSP00000293800.6:n.369-80T>C
ENST00000381074.8:c.240-29T>C	ENSP00000370464.4:n.240-29T>C
ENST00000433363.6:c.369-29T>C	ENSP00000406220.2:n.369-29T>C
ENST00000572094.1:c.*119-29T>C	ENSP00000461495.1:n.*119-29T>C
ENST00000572352.5:c.258-29T>C	ENSP00000461622.1:n.258-29T>C
ENST00000573648.5:c.369-29T>C	ENSP00000459372.1:n.369-29T>C
ENST00000574824.5:n.1473T>C
ENST00000575230.1:c.*215-29T>C	ENSP00000460903.1:n.*215-29T>C
ENST00000576323.1:n.399-29T>C
NM_001143838.2:c.369-29T>C	NP_001137310.1:n.369-29T>C
NM_001284509.1:c.369-80T>C	NP_001271438.1:n.369-80T>C
NM_001284510.1:c.240-29T>C	NP_001271439.1:n.240-29T>C
NM_177550.4:c.369-29T>C , LRG_1020t1:c.369-29T>C	NP_808218.1:n.369-29T>C
XM_006721504.2:c.258-29T>C	XP_006721567.1:n.258-29T>C
XM_011523795.1:c.369-29T>C	XP_011522097.1:n.369-29T>C
XM_011523795.3:c.369-29T>C	XP_011522097.1:n.369-29T>C
NM_001143838.3:c.369-29T>C	NP_001137310.1:n.369-29T>C
NM_001284509.2:c.369-80T>C	NP_001271438.1:n.369-80T>C
NM_001284510.2:c.240-29T>C	NP_001271439.1:n.240-29T>C
NM_177550.5:c.369-29T>C MANE Select	NP_808218.1:n.369-29T>C