Canonical Allele Identifier: CA2245482569

Gene: SLC13A5 C17orf100 ALOX15P1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6687534C= , CM000679.2:g.6687534C=	GRCh38
NC_000017.10:g.6590853C= , CM000679.1:g.6590853C=	GRCh37
NC_000017.9:g.6531577C=	NCBI36
NG_034220.1:g.30888G= , LRG_1020:g.30888G=

Transcript Alleles

HGVS	Amino-acid Change
NM_177550.5:c.1570G= (SLC13A5) MANE Select	NP_808218.1:p.Asp524=
ENST00000433363.7:c.1570G= (SLC13A5) MANE Select	ENSP00000406220.2:p.Asp524=
NM_001143838.2:c.1438-1196G= (SLC13A5)	NP_001137310.1:n.1438-1196G=
NM_001143838.3:c.1438-1196G= (SLC13A5)	NP_001137310.1:n.1438-1196G=
NM_001284509.1:c.1519G= (SLC13A5)	NP_001271438.1:p.Asp507=
NM_001284509.2:c.1519G= (SLC13A5)	NP_001271438.1:p.Asp507=
NM_001284510.1:c.1441G= (SLC13A5)	NP_001271439.1:p.Asp481=
NM_001284510.2:c.1441G= (SLC13A5)	NP_001271439.1:p.Asp481=
NM_177550.4:c.1570G= , LRG_1020t1:c.1570G= (SLC13A5)	NP_808218.1:p.Asp524=
ENST00000293800.10:c.1519G= (SLC13A5)	ENSP00000293800.6:p.Asp507=
ENST00000381074.8:c.1441G= (SLC13A5)	ENSP00000370464.4:p.Asp481=
ENST00000433363.6:c.1570G= (SLC13A5)	ENSP00000406220.2:p.Asp524=
ENST00000570687.1:c.239G= (SLC13A5)
ENST00000573648.5:c.1438-1196G= (SLC13A5)	ENSP00000459372.1:n.1438-1196G=
ENST00000574580.2:n.2587G= (SLC13A5)
ENST00000634558.1:n.511-2342C= (ALOX15P1)
ENST00000634823.1:n.265-5331C= (ALOX15P1)
ENST00000635042.1:n.725-5331C= (C17orf100)
XM_006721504.2:c.1459G= (SLC13A5)	XP_006721567.1:p.Asp487=
XM_011523795.3:c.*243G= (SLC13A5)	XP_011522097.1:n.*243G=