Canonical Allele Identifier: CA497596269

Gene: SLC13A5

Linked Data

• gnomAD v4: 17-6695784-G-T
• MyVariant Identifiers: chr17:g.6599103G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695784G>T , CM000679.2:g.6695784G>T	GRCh38
NC_000017.10:g.6599103G>T , CM000679.1:g.6599103G>T	GRCh37
NC_000017.9:g.6539827G>T	NCBI36
NG_034220.1:g.22638C>A , LRG_1020:g.22638C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.997C>A MANE Select	ENSP00000406220.2:p.Arg333=
ENST00000293800.10:c.946C>A	ENSP00000293800.6:p.Arg316=
ENST00000381074.8:c.868C>A	ENSP00000370464.4:p.Arg290=
ENST00000433363.6:c.997C>A	ENSP00000406220.2:p.Arg333=
ENST00000572727.1:n.106C>A
ENST00000573648.5:c.997C>A	ENSP00000459372.1:p.Arg333=
ENST00000574824.5:n.2130C>A
NM_001143838.2:c.997C>A	NP_001137310.1:p.Arg333=
NM_001284509.1:c.946C>A	NP_001271438.1:p.Arg316=
NM_001284510.1:c.868C>A	NP_001271439.1:p.Arg290=
NM_177550.4:c.997C>A , LRG_1020t1:c.997C>A	NP_808218.1:p.Arg333=
XM_006721504.2:c.886C>A	XP_006721567.1:p.Arg296=
XM_011523795.1:c.997C>A	XP_011522097.1:p.Arg333=
XM_011523795.3:c.997C>A	XP_011522097.1:p.Arg333=
NM_001143838.3:c.997C>A	NP_001137310.1:p.Arg333=
NM_001284509.2:c.946C>A	NP_001271438.1:p.Arg316=
NM_001284510.2:c.868C>A	NP_001271439.1:p.Arg290=
NM_177550.5:c.997C>A MANE Select	NP_808218.1:p.Arg333=