Canonical Allele Identifier: CA1727518283

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121894G= , CM000669.2:g.96121894G=	GRCh38
NC_000007.13:g.95751206G= , CM000669.1:g.95751206G=	GRCh37
NC_000007.12:g.95589142G=	NCBI36
NG_012247.1:g.205254C=
NG_012247.2:g.205254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1695C= MANE Select	ENSP00000265631.6:p.Cys565=
ENST00000265631.9:c.1695C=	ENSP00000265631.5:p.Cys565=
ENST00000416240.6:c.1698C=	ENSP00000400101.2:p.Cys566=
ENST00000494085.1:n.105C=
NM_001160210.1:c.1698C=	NP_001153682.1:p.Cys566=
NM_014251.2:c.1695C=	NP_055066.1:p.Cys565=
NR_027662.1:n.1770C=
XM_006715831.2:c.1728C=	XP_006715894.1:p.Cys576=
XM_011515728.1:c.843C=	XP_011514030.1:p.Cys281=
XM_006715831.4:c.1728C=	XP_006715894.1:p.Cys576=
XM_017011663.1:c.1686C=	XP_016867152.1:p.Cys562=
XM_017011664.2:c.843C=	XP_016867153.1:p.Cys281=
XM_017011665.1:c.843C=	XP_016867154.1:p.Cys281=
XR_001744525.2:n.1941C=
XR_002956405.1:n.2499C=
NM_014251.3:c.1695C= MANE Select	NP_055066.1:p.Cys565=
NR_027662.2:n.1721C=
NM_001160210.2:c.1698C=	NP_001153682.1:p.Cys566=