Canonical Allele Identifier: CA1727518353

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121916G= , CM000669.2:g.96121916G=	GRCh38
NC_000007.13:g.95751228G= , CM000669.1:g.95751228G=	GRCh37
NC_000007.12:g.95589164G=	NCBI36
NG_012247.1:g.205232C=
NG_012247.2:g.205232C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1673C= MANE Select	ENSP00000265631.6:p.Thr558=
ENST00000265631.9:c.1673C=	ENSP00000265631.5:p.Thr558=
ENST00000416240.6:c.1676C=	ENSP00000400101.2:p.Thr559=
ENST00000494085.1:n.83C=
NM_001160210.1:c.1676C=	NP_001153682.1:p.Thr559=
NM_014251.2:c.1673C=	NP_055066.1:p.Thr558=
NR_027662.1:n.1748C=
XM_006715831.2:c.1706C=	XP_006715894.1:p.Thr569=
XM_011515728.1:c.821C=	XP_011514030.1:p.Thr274=
XM_006715831.4:c.1706C=	XP_006715894.1:p.Thr569=
XM_017011663.1:c.1664C=	XP_016867152.1:p.Thr555=
XM_017011664.2:c.821C=	XP_016867153.1:p.Thr274=
XM_017011665.1:c.821C=	XP_016867154.1:p.Thr274=
XR_001744525.2:n.1919C=
XR_002956405.1:n.2477C=
NM_014251.3:c.1673C= MANE Select	NP_055066.1:p.Thr558=
NR_027662.2:n.1699C=
NM_001160210.2:c.1676C=	NP_001153682.1:p.Thr559=