Canonical Allele Identifier: CA1727615615

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96321942C= , CM000669.2:g.96321942C=	GRCh38
NC_000007.13:g.95951254C= , CM000669.1:g.95951254C=	GRCh37
NC_000007.12:g.95789190C=	NCBI36
NG_012247.1:g.5206G=
NG_012247.2:g.5206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.15G= MANE Select	ENSP00000265631.6:p.Lys5=
ENST00000265631.9:c.15G=	ENSP00000265631.5:p.Lys5=
ENST00000416240.6:c.15G=	ENSP00000400101.2:p.Lys5=
ENST00000472162.2:c.15G=	ENSP00000473505.1:p.Lys5=
NM_001160210.1:c.15G=	NP_001153682.1:p.Lys5=
NM_014251.2:c.15G=	NP_055066.1:p.Lys5=
NR_027662.1:n.206G=
XM_011515727.3:c.-107G=	XP_011514029.1:n.-107G=
XM_017011664.2:c.-744G=	XP_016867153.1:n.-744G=
XM_017011665.1:c.-628G=	XP_016867154.1:n.-628G=
XR_001744525.2:n.186G=
XR_002956405.1:n.174G=
NM_014251.3:c.15G= MANE Select	NP_055066.1:p.Lys5=
NR_027662.2:n.157G=
NM_001160210.2:c.15G=	NP_001153682.1:p.Lys5=