Canonical Allele Identifier: CA1727574860

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184183A= , CM000669.2:g.96184183A=	GRCh38
NC_000007.13:g.95813495A= , CM000669.1:g.95813495A=	GRCh37
NC_000007.12:g.95651431A=	NCBI36
NG_012247.1:g.142965T=
NG_012247.2:g.142965T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1177+94T= MANE Select	ENSP00000265631.6:n.1177+94T=
ENST00000265631.9:c.1177+94T=	ENSP00000265631.5:n.1177+94T=
ENST00000416240.6:c.1180+94T=	ENSP00000400101.2:n.1180+94T=
ENST00000484495.5:n.330+94T=
ENST00000490072.5:n.244+94T=
ENST00000492869.1:n.298+94T=
NM_001160210.1:c.1180+94T=	NP_001153682.1:n.1180+94T=
NM_014251.2:c.1177+94T=	NP_055066.1:n.1177+94T=
NR_027662.1:n.1252+94T=
XM_006715831.2:c.1210+94T=	XP_006715894.1:n.1210+94T=
XM_011515727.1:c.1210+94T=	XP_011514029.1:n.1210+94T=
XM_011515728.1:c.325+94T=	XP_011514030.1:n.325+94T=
XM_006715831.4:c.1210+94T=	XP_006715894.1:n.1210+94T=
XM_011515727.3:c.1210+94T=	XP_011514029.1:n.1210+94T=
XM_017011663.1:c.1168+94T=	XP_016867152.1:n.1168+94T=
XM_017011664.2:c.325+94T=	XP_016867153.1:n.325+94T=
XM_017011665.1:c.325+94T=	XP_016867154.1:n.325+94T=
XR_001744525.2:n.1348+94T=
XR_002956405.1:n.1981+94T=
NM_014251.3:c.1177+94T= MANE Select	NP_055066.1:n.1177+94T=
NR_027662.2:n.1203+94T=
NM_001160210.2:c.1180+94T=	NP_001153682.1:n.1180+94T=