Canonical Allele Identifier: CA497596306

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6599155C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695836C>A , CM000679.2:g.6695836C>A	GRCh38
NC_000017.10:g.6599155C>A , CM000679.1:g.6599155C>A	GRCh37
NC_000017.9:g.6539879C>A	NCBI36
NG_034220.1:g.22586G>T , LRG_1020:g.22586G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.945G>T MANE Select	ENSP00000406220.2:p.Ala315=
ENST00000293800.10:c.894G>T	ENSP00000293800.6:p.Ala298=
ENST00000381074.8:c.816G>T	ENSP00000370464.4:p.Ala272=
ENST00000433363.6:c.945G>T	ENSP00000406220.2:p.Ala315=
ENST00000572094.1:c.*695G>T	ENSP00000461495.1:n.*695G>T
ENST00000572727.1:n.54G>T
ENST00000573648.5:c.945G>T	ENSP00000459372.1:p.Ala315=
ENST00000574824.5:n.2078G>T
NM_001143838.2:c.945G>T	NP_001137310.1:p.Ala315=
NM_001284509.1:c.894G>T	NP_001271438.1:p.Ala298=
NM_001284510.1:c.816G>T	NP_001271439.1:p.Ala272=
NM_177550.4:c.945G>T , LRG_1020t1:c.945G>T	NP_808218.1:p.Ala315=
XM_006721504.2:c.834G>T	XP_006721567.1:p.Ala278=
XM_011523795.1:c.945G>T	XP_011522097.1:p.Ala315=
XM_011523795.3:c.945G>T	XP_011522097.1:p.Ala315=
NM_001143838.3:c.945G>T	NP_001137310.1:p.Ala315=
NM_001284509.2:c.894G>T	NP_001271438.1:p.Ala298=
NM_001284510.2:c.816G>T	NP_001271439.1:p.Ala272=
NM_177550.5:c.945G>T MANE Select	NP_808218.1:p.Ala315=