Canonical Allele Identifier: CA2578945819

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121417G>T , CM000669.2:g.96121417G>T	GRCh38
NC_000007.13:g.95750729G>T , CM000669.1:g.95750729G>T	GRCh37
NC_000007.12:g.95588665G>T	NCBI36
NG_012247.1:g.205731C>A
NG_012247.2:g.205731C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-40C>A MANE Select	ENSP00000265631.6:n.1842-40C>A
ENST00000265631.9:c.1842-40C>A	ENSP00000265631.5:n.1842-40C>A
ENST00000416240.6:c.1845-40C>A	ENSP00000400101.2:n.1845-40C>A
ENST00000494085.1:n.345-40C>A
NM_001160210.1:c.1845-40C>A	NP_001153682.1:n.1845-40C>A
NM_014251.2:c.1842-40C>A	NP_055066.1:n.1842-40C>A
NR_027662.1:n.1917-40C>A
XM_006715831.2:c.1875-40C>A	XP_006715894.1:n.1875-40C>A
XM_011515728.1:c.990-40C>A	XP_011514030.1:n.990-40C>A
XM_006715831.4:c.1875-40C>A	XP_006715894.1:n.1875-40C>A
XM_017011663.1:c.1833-40C>A	XP_016867152.1:n.1833-40C>A
XM_017011664.2:c.990-40C>A	XP_016867153.1:n.990-40C>A
XM_017011665.1:c.990-40C>A	XP_016867154.1:n.990-40C>A
XR_001744525.2:n.2088-40C>A
XR_002956405.1:n.2646-40C>A
NM_014251.3:c.1842-40C>A MANE Select	NP_055066.1:n.1842-40C>A
NR_027662.2:n.1868-40C>A
NM_001160210.2:c.1845-40C>A	NP_001153682.1:n.1845-40C>A