Canonical Allele Identifier: CA1727518369

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121919G= , CM000669.2:g.96121919G=	GRCh38
NC_000007.13:g.95751231G= , CM000669.1:g.95751231G=	GRCh37
NC_000007.12:g.95589167G=	NCBI36
NG_012247.1:g.205229C=
NG_012247.2:g.205229C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1670C= MANE Select	ENSP00000265631.6:p.Thr557=
ENST00000265631.9:c.1670C=	ENSP00000265631.5:p.Thr557=
ENST00000416240.6:c.1673C=	ENSP00000400101.2:p.Thr558=
ENST00000494085.1:n.80C=
NM_001160210.1:c.1673C=	NP_001153682.1:p.Thr558=
NM_014251.2:c.1670C=	NP_055066.1:p.Thr557=
NR_027662.1:n.1745C=
XM_006715831.2:c.1703C=	XP_006715894.1:p.Thr568=
XM_011515728.1:c.818C=	XP_011514030.1:p.Thr273=
XM_006715831.4:c.1703C=	XP_006715894.1:p.Thr568=
XM_017011663.1:c.1661C=	XP_016867152.1:p.Thr554=
XM_017011664.2:c.818C=	XP_016867153.1:p.Thr273=
XM_017011665.1:c.818C=	XP_016867154.1:p.Thr273=
XR_001744525.2:n.1916C=
XR_002956405.1:n.2474C=
NM_014251.3:c.1670C= MANE Select	NP_055066.1:p.Thr557=
NR_027662.2:n.1696C=
NM_001160210.2:c.1673C=	NP_001153682.1:p.Thr558=