Canonical Allele Identifier: CA397745061

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6599250A>C (hg19) ; chr17:g.6695931A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695931A>C , CM000679.2:g.6695931A>C	GRCh38
NC_000017.10:g.6599250A>C , CM000679.1:g.6599250A>C	GRCh37
NC_000017.9:g.6539974A>C	NCBI36
NG_034220.1:g.22491T>G , LRG_1020:g.22491T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.850T>G MANE Select	ENSP00000406220.2:p.Ser284Ala
ENST00000293800.10:c.799T>G	ENSP00000293800.6:p.Ser267Ala
ENST00000381074.8:c.721T>G	ENSP00000370464.4:p.Ser241Ala
ENST00000433363.6:c.850T>G	ENSP00000406220.2:p.Ser284Ala
ENST00000572094.1:c.*600T>G	ENSP00000461495.1:n.*600T>G
ENST00000573648.5:c.850T>G	ENSP00000459372.1:p.Ser284Ala
ENST00000574824.5:n.1983T>G
NM_001143838.2:c.850T>G	NP_001137310.1:p.Ser284Ala
NM_001284509.1:c.799T>G	NP_001271438.1:p.Ser267Ala
NM_001284510.1:c.721T>G	NP_001271439.1:p.Ser241Ala
NM_177550.4:c.850T>G , LRG_1020t1:c.850T>G	NP_808218.1:p.Ser284Ala
XM_006721504.2:c.739T>G	XP_006721567.1:p.Ser247Ala
XM_011523795.1:c.850T>G	XP_011522097.1:p.Ser284Ala
XM_011523795.3:c.850T>G	XP_011522097.1:p.Ser284Ala
NM_001143838.3:c.850T>G	NP_001137310.1:p.Ser284Ala
NM_001284509.2:c.799T>G	NP_001271438.1:p.Ser267Ala
NM_001284510.2:c.721T>G	NP_001271439.1:p.Ser241Ala
NM_177550.5:c.850T>G MANE Select	NP_808218.1:p.Ser284Ala