Canonical Allele Identifier: CA1727575118

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184376G= , CM000669.2:g.96184376G=	GRCh38
NC_000007.13:g.95813688G= , CM000669.1:g.95813688G=	GRCh37
NC_000007.12:g.95651624G=	NCBI36
NG_012247.1:g.142772C=
NG_012247.2:g.142772C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.1078C= MANE Select	NP_055066.1:p.Arg360=
ENST00000265631.10:c.1078C= MANE Select	ENSP00000265631.6:p.Arg360=
NM_001160210.1:c.1081C=	NP_001153682.1:p.Arg361=
NM_001160210.2:c.1081C=	NP_001153682.1:p.Arg361=
NM_014251.2:c.1078C=	NP_055066.1:p.Arg360=
NR_027662.1:n.1153C=
NR_027662.2:n.1104C=
ENST00000265631.9:c.1078C=	ENSP00000265631.5:p.Arg360=
ENST00000416240.6:c.1081C=	ENSP00000400101.2:p.Arg361=
ENST00000484495.5:n.231C=
ENST00000490072.5:n.145C=
ENST00000492869.1:n.199C=
XM_006715831.2:c.1111C=	XP_006715894.1:p.Arg371=
XM_006715831.4:c.1111C=	XP_006715894.1:p.Arg371=
XM_011515727.1:c.1111C=	XP_011514029.1:p.Arg371=
XM_011515727.3:c.1111C=	XP_011514029.1:p.Arg371=
XM_011515728.1:c.226C=	XP_011514030.1:p.Arg76=
XM_017011663.1:c.1069C=	XP_016867152.1:p.Arg357=
XM_017011664.2:c.226C=	XP_016867153.1:p.Arg76=
XM_017011665.1:c.226C=	XP_016867154.1:p.Arg76=
XR_001744525.2:n.1249C=
XR_002956405.1:n.1882C=