Canonical Allele Identifier: CA1727517886

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121703A= , CM000669.2:g.96121703A=	GRCh38
NC_000007.13:g.95751015A= , CM000669.1:g.95751015A=	GRCh37
NC_000007.12:g.95588951A=	NCBI36
NG_012247.1:g.205445T=
NG_012247.2:g.205445T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1793T= MANE Select	ENSP00000265631.6:p.Leu598=
ENST00000265631.9:c.1793T=	ENSP00000265631.5:p.Leu598=
ENST00000416240.6:c.1796T=	ENSP00000400101.2:p.Leu599=
ENST00000494085.1:n.296T=
NM_001160210.1:c.1796T=	NP_001153682.1:p.Leu599=
NM_014251.2:c.1793T=	NP_055066.1:p.Leu598=
NR_027662.1:n.1868T=
XM_006715831.2:c.1826T=	XP_006715894.1:p.Leu609=
XM_011515728.1:c.941T=	XP_011514030.1:p.Leu314=
XM_006715831.4:c.1826T=	XP_006715894.1:p.Leu609=
XM_017011663.1:c.1784T=	XP_016867152.1:p.Leu595=
XM_017011664.2:c.941T=	XP_016867153.1:p.Leu314=
XM_017011665.1:c.941T=	XP_016867154.1:p.Leu314=
XR_001744525.2:n.2039T=
XR_002956405.1:n.2597T=
NM_014251.3:c.1793T= MANE Select	NP_055066.1:p.Leu598=
NR_027662.2:n.1819T=
NM_001160210.2:c.1796T=	NP_001153682.1:p.Leu599=