Canonical Allele Identifier: CA774266011

Gene: SLC13A5 C17orf100 ALOX15P1

Linked Data

• dbSNP Id: rs1326367305
• gnomAD v3: 17-6687804-A-G
• gnomAD v4: 17-6687804-A-G
• MyVariant Identifiers: chr17:g.6591123A>G (hg19) ; chr17:g.6687804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6687804A>G , CM000679.2:g.6687804A>G	GRCh38
NC_000017.10:g.6591123A>G , CM000679.1:g.6591123A>G	GRCh37
NC_000017.9:g.6531847A>G	NCBI36
NG_034220.1:g.30618T>C , LRG_1020:g.30618T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1438-138T>C (SLC13A5) MANE Select	ENSP00000406220.2:n.1438-138T>C
ENST00000635042.1:n.725-5061A>G (C17orf100)
ENST00000293800.10:c.1387-138T>C (SLC13A5)	ENSP00000293800.6:n.1387-138T>C
ENST00000381074.8:c.1309-138T>C (SLC13A5)	ENSP00000370464.4:n.1309-138T>C
ENST00000433363.6:c.1438-138T>C (SLC13A5)	ENSP00000406220.2:n.1438-138T>C
ENST00000570687.1:c.107-138T>C (SLC13A5)
ENST00000573648.5:c.1438-1466T>C (SLC13A5)	ENSP00000459372.1:n.1438-1466T>C
ENST00000574580.2:n.2317T>C (SLC13A5)
ENST00000634558.1:n.511-2072A>G (ALOX15P1)
ENST00000634823.1:n.265-5061A>G (ALOX15P1)
NM_001143838.2:c.1438-1466T>C (SLC13A5)	NP_001137310.1:n.1438-1466T>C
NM_001284509.1:c.1387-138T>C (SLC13A5)	NP_001271438.1:n.1387-138T>C
NM_001284510.1:c.1309-138T>C (SLC13A5)	NP_001271439.1:n.1309-138T>C
NM_177550.4:c.1438-138T>C , LRG_1020t1:c.1438-138T>C (SLC13A5)	NP_808218.1:n.1438-138T>C
XM_006721504.2:c.1327-138T>C (SLC13A5)	XP_006721567.1:n.1327-138T>C
XM_011523795.1:c.1470T>C (SLC13A5)	XP_011522097.1:p.Arg490=
XM_011523795.3:c.1470T>C (SLC13A5)	XP_011522097.1:p.Arg490=
NM_001143838.3:c.1438-1466T>C (SLC13A5)	NP_001137310.1:n.1438-1466T>C
NM_001284509.2:c.1387-138T>C (SLC13A5)	NP_001271438.1:n.1387-138T>C
NM_001284510.2:c.1309-138T>C (SLC13A5)	NP_001271439.1:n.1309-138T>C
NM_177550.5:c.1438-138T>C (SLC13A5) MANE Select	NP_808218.1:n.1438-138T>C