Canonical Allele Identifier: CA1727583742

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193102G= , CM000669.2:g.96193102G=	GRCh38
NC_000007.13:g.95822414G= , CM000669.1:g.95822414G=	GRCh37
NC_000007.12:g.95660350G=	NCBI36
NG_012247.1:g.134046C=
NG_012247.2:g.134046C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.550C= MANE Select	ENSP00000265631.6:p.Arg184=
ENST00000265631.9:c.550C=	ENSP00000265631.5:p.Arg184=
ENST00000416240.6:c.550C=	ENSP00000400101.2:p.Arg184=
NM_001160210.1:c.550C=	NP_001153682.1:p.Arg184=
NM_014251.2:c.550C=	NP_055066.1:p.Arg184=
NR_027662.1:n.625C=
XM_006715831.2:c.583C=	XP_006715894.1:p.Arg195=
XM_011515727.1:c.583C=	XP_011514029.1:p.Arg195=
XM_006715831.4:c.583C=	XP_006715894.1:p.Arg195=
XM_011515727.3:c.583C=	XP_011514029.1:p.Arg195=
XM_017011663.1:c.541C=	XP_016867152.1:p.Arg181=
XM_017011664.2:c.-209C=	XP_016867153.1:n.-209C=
XM_017011665.1:c.-209C=	XP_016867154.1:n.-209C=
XR_001744525.2:n.721C=
XR_002956405.1:n.863C=
NM_014251.3:c.550C= MANE Select	NP_055066.1:p.Arg184=
NR_027662.2:n.576C=
NM_001160210.2:c.550C=	NP_001153682.1:p.Arg184=