Canonical Allele Identifier: CA1727517556

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121526A= , CM000669.2:g.96121526A=	GRCh38
NC_000007.13:g.95750838A= , CM000669.1:g.95750838A=	GRCh37
NC_000007.12:g.95588774A=	NCBI36
NG_012247.1:g.205622T=
NG_012247.2:g.205622T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1841+129T= MANE Select	ENSP00000265631.6:n.1841+129T=
ENST00000265631.9:c.1841+129T=	ENSP00000265631.5:n.1841+129T=
ENST00000416240.6:c.1844+129T=	ENSP00000400101.2:n.1844+129T=
ENST00000494085.1:n.344+129T=
NM_001160210.1:c.1844+129T=	NP_001153682.1:n.1844+129T=
NM_014251.2:c.1841+129T=	NP_055066.1:n.1841+129T=
NR_027662.1:n.1916+129T=
XM_006715831.2:c.1874+129T=	XP_006715894.1:n.1874+129T=
XM_011515728.1:c.989+129T=	XP_011514030.1:n.989+129T=
XM_006715831.4:c.1874+129T=	XP_006715894.1:n.1874+129T=
XM_017011663.1:c.1832+129T=	XP_016867152.1:n.1832+129T=
XM_017011664.2:c.989+129T=	XP_016867153.1:n.989+129T=
XM_017011665.1:c.989+129T=	XP_016867154.1:n.989+129T=
XR_001744525.2:n.2087+129T=
XR_002956405.1:n.2645+129T=
NM_014251.3:c.1841+129T= MANE Select	NP_055066.1:n.1841+129T=
NR_027662.2:n.1867+129T=
NM_001160210.2:c.1844+129T=	NP_001153682.1:n.1844+129T=