Canonical Allele Identifier: CA774265798

Gene: SLC13A5 C17orf100 ALOX15P1

Linked Data

• dbSNP Id: rs1178661973
• MyVariant Identifiers: chr17:g.6590921_6590922insC (hg19) ; chr17:g.6687602_6687603insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6687603dup , CM000679.2:g.6687603dup	GRCh38
NC_000017.10:g.6590922dup , CM000679.1:g.6590922dup	GRCh37
NC_000017.9:g.6531646dup	NCBI36
NG_034220.1:g.30819dup , LRG_1020:g.30819dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1501dup (SLC13A5) MANE Select	ENSP00000406220.2:p.Ala501GlyfsTer24
ENST00000635042.1:n.725-5262dup (C17orf100)
ENST00000293800.10:c.1450dup (SLC13A5)	ENSP00000293800.6:p.Ala484GlyfsTer24
ENST00000381074.8:c.1372dup (SLC13A5)	ENSP00000370464.4:p.Ala458GlyfsTer24
ENST00000433363.6:c.1501dup (SLC13A5)	ENSP00000406220.2:p.Ala501GlyfsTer24
ENST00000570687.1:c.170dup (SLC13A5)
ENST00000573648.5:c.1438-1265dup (SLC13A5)	ENSP00000459372.1:n.1438-1265dup
ENST00000574580.2:n.2518dup (SLC13A5)
ENST00000634558.1:n.511-2273dup (ALOX15P1)
ENST00000634823.1:n.265-5262dup (ALOX15P1)
NM_001143838.2:c.1438-1265dup (SLC13A5)	NP_001137310.1:n.1438-1265dup
NM_001284509.1:c.1450dup (SLC13A5)	NP_001271438.1:p.Ala484GlyfsTer24
NM_001284510.1:c.1372dup (SLC13A5)	NP_001271439.1:p.Ala458GlyfsTer24
NM_177550.4:c.1501dup , LRG_1020t1:c.1501dup (SLC13A5)	NP_808218.1:p.Ala501GlyfsTer24
XM_006721504.2:c.1390dup (SLC13A5)	XP_006721567.1:p.Ala464GlyfsTer24
XM_011523795.3:c.*174dup (SLC13A5)	XP_011522097.1:n.*174dup
NM_001143838.3:c.1438-1265dup (SLC13A5)	NP_001137310.1:n.1438-1265dup
NM_001284509.2:c.1450dup (SLC13A5)	NP_001271438.1:p.Ala484GlyfsTer24
NM_001284510.2:c.1372dup (SLC13A5)	NP_001271439.1:p.Ala458GlyfsTer24
NM_177550.5:c.1501dup (SLC13A5) MANE Select	NP_808218.1:p.Ala501GlyfsTer24