Canonical Allele Identifier: CA1727517881

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121700G= , CM000669.2:g.96121700G=	GRCh38
NC_000007.13:g.95751012G= , CM000669.1:g.95751012G=	GRCh37
NC_000007.12:g.95588948G=	NCBI36
NG_012247.1:g.205448C=
NG_012247.2:g.205448C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1796C= MANE Select	ENSP00000265631.6:p.Thr599=
ENST00000265631.9:c.1796C=	ENSP00000265631.5:p.Thr599=
ENST00000416240.6:c.1799C=	ENSP00000400101.2:p.Thr600=
ENST00000494085.1:n.299C=
NM_001160210.1:c.1799C=	NP_001153682.1:p.Thr600=
NM_014251.2:c.1796C=	NP_055066.1:p.Thr599=
NR_027662.1:n.1871C=
XM_006715831.2:c.1829C=	XP_006715894.1:p.Thr610=
XM_011515728.1:c.944C=	XP_011514030.1:p.Thr315=
XM_006715831.4:c.1829C=	XP_006715894.1:p.Thr610=
XM_017011663.1:c.1787C=	XP_016867152.1:p.Thr596=
XM_017011664.2:c.944C=	XP_016867153.1:p.Thr315=
XM_017011665.1:c.944C=	XP_016867154.1:p.Thr315=
XR_001744525.2:n.2042C=
XR_002956405.1:n.2600C=
NM_014251.3:c.1796C= MANE Select	NP_055066.1:p.Thr599=
NR_027662.2:n.1822C=
NM_001160210.2:c.1799C=	NP_001153682.1:p.Thr600=