Canonical Allele Identifier: CA4353156

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189639C>T , CM000669.2:g.96189639C>T	GRCh38
NC_000007.13:g.95818951C>T , CM000669.1:g.95818951C>T	GRCh37
NC_000007.12:g.95656887C>T	NCBI36
NG_012247.1:g.137509G>A
NG_012247.2:g.137509G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.790G>A MANE Select	NP_055066.1:p.Val264Ile
ENST00000265631.10:c.790G>A MANE Select	ENSP00000265631.6:p.Val264Ile
NM_001160210.1:c.790G>A	NP_001153682.1:p.Val264Ile
NM_001160210.2:c.790G>A	NP_001153682.1:p.Val264Ile
NM_014251.2:c.790G>A	NP_055066.1:p.Val264Ile
NR_027662.1:n.865G>A
NR_027662.2:n.816G>A
ENST00000265631.9:c.790G>A	ENSP00000265631.5:p.Val264Ile
ENST00000416240.6:c.790G>A	ENSP00000400101.2:p.Val264Ile
XM_006715831.2:c.823G>A	XP_006715894.1:p.Val275Ile
XM_006715831.4:c.823G>A	XP_006715894.1:p.Val275Ile
XM_011515727.1:c.823G>A	XP_011514029.1:p.Val275Ile
XM_011515727.3:c.823G>A	XP_011514029.1:p.Val275Ile
XM_011515728.1:c.-4-261G>A	XP_011514030.1:n.-4-261G>A
XM_017011663.1:c.781G>A	XP_016867152.1:p.Val261Ile
XM_017011664.2:c.-4-261G>A	XP_016867153.1:n.-4-261G>A
XM_017011665.1:c.-4-261G>A	XP_016867154.1:n.-4-261G>A
XR_001744525.2:n.961G>A
XR_002956405.1:n.1103G>A