Canonical Allele Identifier: CA1727518010

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121740C= , CM000669.2:g.96121740C=	GRCh38
NC_000007.13:g.95751052C= , CM000669.1:g.95751052C=	GRCh37
NC_000007.12:g.95588988C=	NCBI36
NG_012247.1:g.205408G=
NG_012247.2:g.205408G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1756G= MANE Select	ENSP00000265631.6:p.Val586=
ENST00000265631.9:c.1756G=	ENSP00000265631.5:p.Val586=
ENST00000416240.6:c.1759G=	ENSP00000400101.2:p.Val587=
ENST00000494085.1:n.259G=
NM_001160210.1:c.1759G=	NP_001153682.1:p.Val587=
NM_014251.2:c.1756G=	NP_055066.1:p.Val586=
NR_027662.1:n.1831G=
XM_006715831.2:c.1789G=	XP_006715894.1:p.Val597=
XM_011515728.1:c.904G=	XP_011514030.1:p.Val302=
XM_006715831.4:c.1789G=	XP_006715894.1:p.Val597=
XM_017011663.1:c.1747G=	XP_016867152.1:p.Val583=
XM_017011664.2:c.904G=	XP_016867153.1:p.Val302=
XM_017011665.1:c.904G=	XP_016867154.1:p.Val302=
XR_001744525.2:n.2002G=
XR_002956405.1:n.2560G=
NM_014251.3:c.1756G= MANE Select	NP_055066.1:p.Val586=
NR_027662.2:n.1782G=
NM_001160210.2:c.1759G=	NP_001153682.1:p.Val587=