Canonical Allele Identifier: CA1727565262

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96170045G= , CM000669.2:g.96170045G=	GRCh38
NC_000007.13:g.95799357G= , CM000669.1:g.95799357G=	GRCh37
NC_000007.12:g.95637293G=	NCBI36
NG_012247.1:g.157103C=
NG_012247.2:g.157103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1311C= MANE Select	ENSP00000265631.6:p.Cys437=
ENST00000265631.9:c.1311C=	ENSP00000265631.5:p.Cys437=
ENST00000416240.6:c.1314C=	ENSP00000400101.2:p.Cys438=
ENST00000484495.5:n.464C=
ENST00000490072.5:n.378C=
ENST00000492869.1:n.432C=
NM_001160210.1:c.1314C=	NP_001153682.1:p.Cys438=
NM_014251.2:c.1311C=	NP_055066.1:p.Cys437=
NR_027662.1:n.1386C=
XM_006715831.2:c.1344C=	XP_006715894.1:p.Cys448=
XM_011515727.1:c.1344C=	XP_011514029.1:p.Cys448=
XM_011515728.1:c.459C=	XP_011514030.1:p.Cys153=
XM_006715831.4:c.1344C=	XP_006715894.1:p.Cys448=
XM_011515727.3:c.1344C=	XP_011514029.1:p.Cys448=
XM_017011663.1:c.1302C=	XP_016867152.1:p.Cys434=
XM_017011664.2:c.459C=	XP_016867153.1:p.Cys153=
XM_017011665.1:c.459C=	XP_016867154.1:p.Cys153=
XR_001744525.2:n.1482C=
XR_002956405.1:n.2115C=
NM_014251.3:c.1311C= MANE Select	NP_055066.1:p.Cys437=
NR_027662.2:n.1337C=
NM_001160210.2:c.1314C=	NP_001153682.1:p.Cys438=