Canonical Allele Identifier: CA1727517818

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121683G= , CM000669.2:g.96121683G=	GRCh38
NC_000007.13:g.95750995G= , CM000669.1:g.95750995G=	GRCh37
NC_000007.12:g.95588931G=	NCBI36
NG_012247.1:g.205465C=
NG_012247.2:g.205465C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1813C= MANE Select	ENSP00000265631.6:p.Arg605=
ENST00000265631.9:c.1813C=	ENSP00000265631.5:p.Arg605=
ENST00000416240.6:c.1816C=	ENSP00000400101.2:p.Arg606=
ENST00000494085.1:n.316C=
NM_001160210.1:c.1816C=	NP_001153682.1:p.Arg606=
NM_014251.2:c.1813C=	NP_055066.1:p.Arg605=
NR_027662.1:n.1888C=
XM_006715831.2:c.1846C=	XP_006715894.1:p.Arg616=
XM_011515728.1:c.961C=	XP_011514030.1:p.Arg321=
XM_006715831.4:c.1846C=	XP_006715894.1:p.Arg616=
XM_017011663.1:c.1804C=	XP_016867152.1:p.Arg602=
XM_017011664.2:c.961C=	XP_016867153.1:p.Arg321=
XM_017011665.1:c.961C=	XP_016867154.1:p.Arg321=
XR_001744525.2:n.2059C=
XR_002956405.1:n.2617C=
NM_014251.3:c.1813C= MANE Select	NP_055066.1:p.Arg605=
NR_027662.2:n.1839C=
NM_001160210.2:c.1816C=	NP_001153682.1:p.Arg606=