Canonical Allele Identifier: CA497596363

Gene: SLC13A5

Linked Data

• gnomAD v4: 17-6695938-A-G
• MyVariant Identifiers: chr17:g.6599257A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695938A>G , CM000679.2:g.6695938A>G	GRCh38
NC_000017.10:g.6599257A>G , CM000679.1:g.6599257A>G	GRCh37
NC_000017.9:g.6539981A>G	NCBI36
NG_034220.1:g.22484T>C , LRG_1020:g.22484T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.843T>C MANE Select	ENSP00000406220.2:p.Phe281=
ENST00000293800.10:c.792T>C	ENSP00000293800.6:p.Phe264=
ENST00000381074.8:c.714T>C	ENSP00000370464.4:p.Phe238=
ENST00000433363.6:c.843T>C	ENSP00000406220.2:p.Phe281=
ENST00000572094.1:c.*593T>C	ENSP00000461495.1:n.*593T>C
ENST00000573648.5:c.843T>C	ENSP00000459372.1:p.Phe281=
ENST00000574824.5:n.1976T>C
NM_001143838.2:c.843T>C	NP_001137310.1:p.Phe281=
NM_001284509.1:c.792T>C	NP_001271438.1:p.Phe264=
NM_001284510.1:c.714T>C	NP_001271439.1:p.Phe238=
NM_177550.4:c.843T>C , LRG_1020t1:c.843T>C	NP_808218.1:p.Phe281=
XM_006721504.2:c.732T>C	XP_006721567.1:p.Phe244=
XM_011523795.1:c.843T>C	XP_011522097.1:p.Phe281=
XM_011523795.3:c.843T>C	XP_011522097.1:p.Phe281=
NM_001143838.3:c.843T>C	NP_001137310.1:p.Phe281=
NM_001284509.2:c.792T>C	NP_001271438.1:p.Phe264=
NM_001284510.2:c.714T>C	NP_001271439.1:p.Phe238=
NM_177550.5:c.843T>C MANE Select	NP_808218.1:p.Phe281=