Canonical Allele Identifier: CA397750111

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6607296G>T (hg19) ; chr17:g.6703977G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6703977G>T , CM000679.2:g.6703977G>T	GRCh38
NC_000017.10:g.6607296G>T , CM000679.1:g.6607296G>T	GRCh37
NC_000017.9:g.6548020G>T	NCBI36
NG_034220.1:g.14445C>A , LRG_1020:g.14445C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.448C>A MANE Select	ENSP00000406220.2:p.Pro150Thr
ENST00000293800.10:c.397C>A	ENSP00000293800.6:p.Pro133Thr
ENST00000381074.8:c.319C>A	ENSP00000370464.4:p.Pro107Thr
ENST00000433363.6:c.448C>A	ENSP00000406220.2:p.Pro150Thr
ENST00000572094.1:c.*198C>A	ENSP00000461495.1:n.*198C>A
ENST00000572352.5:c.337C>A	ENSP00000461622.1:p.Pro113Thr
ENST00000573648.5:c.448C>A	ENSP00000459372.1:p.Pro150Thr
ENST00000574824.5:n.1581C>A
ENST00000576323.1:n.478C>A
NM_001143838.2:c.448C>A	NP_001137310.1:p.Pro150Thr
NM_001284509.1:c.397C>A	NP_001271438.1:p.Pro133Thr
NM_001284510.1:c.319C>A	NP_001271439.1:p.Pro107Thr
NM_177550.4:c.448C>A , LRG_1020t1:c.448C>A	NP_808218.1:p.Pro150Thr
XM_006721504.2:c.337C>A	XP_006721567.1:p.Pro113Thr
XM_011523795.1:c.448C>A	XP_011522097.1:p.Pro150Thr
XM_011523795.3:c.448C>A	XP_011522097.1:p.Pro150Thr
NM_001143838.3:c.448C>A	NP_001137310.1:p.Pro150Thr
NM_001284509.2:c.397C>A	NP_001271438.1:p.Pro133Thr
NM_001284510.2:c.319C>A	NP_001271439.1:p.Pro107Thr
NM_177550.5:c.448C>A MANE Select	NP_808218.1:p.Pro150Thr