Canonical Allele Identifier: CA3223488216

Gene: SLC13A5 C17orf100 ALOX15P1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6693092G= , CM000679.2:g.6693092G=	GRCh38
NC_000017.10:g.6596411G= , CM000679.1:g.6596411G=	GRCh37
NC_000017.9:g.6537135G=	NCBI36
NG_034220.1:g.25330C= , LRG_1020:g.25330C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1227C= (SLC13A5) MANE Select	ENSP00000406220.2:p.Gly409=
ENST00000635042.1:n.952G= (C17orf100)
ENST00000293800.10:c.1176C= (SLC13A5)	ENSP00000293800.6:p.Gly392=
ENST00000381074.8:c.1098C= (SLC13A5)	ENSP00000370464.4:p.Gly366=
ENST00000433363.6:c.1227C= (SLC13A5)	ENSP00000406220.2:p.Gly409=
ENST00000572727.1:n.336C= (SLC13A5)
ENST00000573648.5:c.1227C= (SLC13A5)	ENSP00000459372.1:p.Gly409=
ENST00000634558.1:n.890G= (ALOX15P1)
ENST00000634823.1:n.492G= (ALOX15P1)
NM_001143838.2:c.1227C= (SLC13A5)	NP_001137310.1:p.Gly409=
NM_001284509.1:c.1176C= (SLC13A5)	NP_001271438.1:p.Gly392=
NM_001284510.1:c.1098C= (SLC13A5)	NP_001271439.1:p.Gly366=
NM_177550.4:c.1227C= , LRG_1020t1:c.1227C= (SLC13A5)	NP_808218.1:p.Gly409=
XM_006721504.2:c.1116C= (SLC13A5)	XP_006721567.1:p.Gly372=
XM_011523795.1:c.1227C= (SLC13A5)	XP_011522097.1:p.Gly409=
XM_011523795.3:c.1227C= (SLC13A5)	XP_011522097.1:p.Gly409=
NM_001143838.3:c.1227C= (SLC13A5)	NP_001137310.1:p.Gly409=
NM_001284509.2:c.1176C= (SLC13A5)	NP_001271438.1:p.Gly392=
NM_001284510.2:c.1098C= (SLC13A5)	NP_001271439.1:p.Gly366=
NM_177550.5:c.1227C= (SLC13A5) MANE Select	NP_808218.1:p.Gly409=