Canonical Allele Identifier: CA1727518312

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121908C= , CM000669.2:g.96121908C=	GRCh38
NC_000007.13:g.95751220C= , CM000669.1:g.95751220C=	GRCh37
NC_000007.12:g.95589156C=	NCBI36
NG_012247.1:g.205240G=
NG_012247.2:g.205240G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1681G= MANE Select	ENSP00000265631.6:p.Gly561=
ENST00000265631.9:c.1681G=	ENSP00000265631.5:p.Gly561=
ENST00000416240.6:c.1684G=	ENSP00000400101.2:p.Gly562=
ENST00000494085.1:n.91G=
NM_001160210.1:c.1684G=	NP_001153682.1:p.Gly562=
NM_014251.2:c.1681G=	NP_055066.1:p.Gly561=
NR_027662.1:n.1756G=
XM_006715831.2:c.1714G=	XP_006715894.1:p.Gly572=
XM_011515728.1:c.829G=	XP_011514030.1:p.Gly277=
XM_006715831.4:c.1714G=	XP_006715894.1:p.Gly572=
XM_017011663.1:c.1672G=	XP_016867152.1:p.Gly558=
XM_017011664.2:c.829G=	XP_016867153.1:p.Gly277=
XM_017011665.1:c.829G=	XP_016867154.1:p.Gly277=
XR_001744525.2:n.1927G=
XR_002956405.1:n.2485G=
NM_014251.3:c.1681G= MANE Select	NP_055066.1:p.Gly561=
NR_027662.2:n.1707G=
NM_001160210.2:c.1684G=	NP_001153682.1:p.Gly562=