Canonical Allele Identifier: CA1727574828

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184116_96184117delinsGC , CM000669.2:g.96184116_96184117delinsGC	GRCh38
NC_000007.13:g.95813428_95813429delinsGC , CM000669.1:g.95813428_95813429delinsGC	GRCh37
NC_000007.12:g.95651364_95651365delinsGC	NCBI36
NG_012247.1:g.143031_143032delinsGC
NG_012247.2:g.143031_143032delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1177+160_1177+161delinsGC MANE Select	ENSP00000265631.6:n.1177+160_1177+161delinsGC
ENST00000265631.9:c.1177+160_1177+161delinsGC	ENSP00000265631.5:n.1177+160_1177+161delinsGC
ENST00000416240.6:c.1180+160_1180+161delinsGC	ENSP00000400101.2:n.1180+160_1180+161delinsGC
ENST00000484495.5:n.330+160_330+161delinsGC
ENST00000490072.5:n.244+160_244+161delinsGC
ENST00000492869.1:n.298+160_298+161delinsGC
NM_001160210.1:c.1180+160_1180+161delinsGC	NP_001153682.1:n.1180+160_1180+161delinsGC
NM_014251.2:c.1177+160_1177+161delinsGC	NP_055066.1:n.1177+160_1177+161delinsGC
NR_027662.1:n.1252+160_1252+161delinsGC
XM_006715831.2:c.1210+160_1210+161delinsGC	XP_006715894.1:n.1210+160_1210+161delinsGC
XM_011515727.1:c.1210+160_1210+161delinsGC	XP_011514029.1:n.1210+160_1210+161delinsGC
XM_011515728.1:c.325+160_325+161delinsGC	XP_011514030.1:n.325+160_325+161delinsGC
XM_006715831.4:c.1210+160_1210+161delinsGC	XP_006715894.1:n.1210+160_1210+161delinsGC
XM_011515727.3:c.1210+160_1210+161delinsGC	XP_011514029.1:n.1210+160_1210+161delinsGC
XM_017011663.1:c.1168+160_1168+161delinsGC	XP_016867152.1:n.1168+160_1168+161delinsGC
XM_017011664.2:c.325+160_325+161delinsGC	XP_016867153.1:n.325+160_325+161delinsGC
XM_017011665.1:c.325+160_325+161delinsGC	XP_016867154.1:n.325+160_325+161delinsGC
XR_001744525.2:n.1348+160_1348+161delinsGC
XR_002956405.1:n.1981+160_1981+161delinsGC
NM_014251.3:c.1177+160_1177+161delinsGC MANE Select	NP_055066.1:n.1177+160_1177+161delinsGC
NR_027662.2:n.1203+160_1203+161delinsGC
NM_001160210.2:c.1180+160_1180+161delinsGC	NP_001153682.1:n.1180+160_1180+161delinsGC