Canonical Allele Identifier: CA2695208128

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96170041_96170044del , CM000669.2:g.96170041_96170044del	GRCh38
NC_000007.13:g.95799353_95799356del , CM000669.1:g.95799353_95799356del	GRCh37
NC_000007.12:g.95637289_95637292del	NCBI36
NG_012247.1:g.157107_157110del
NG_012247.2:g.157107_157110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1311+4_1311+7del MANE Select	ENSP00000265631.6:n.1311+4_1311+7del
ENST00000265631.9:c.1311+4_1311+7del	ENSP00000265631.5:n.1311+4_1311+7del
ENST00000416240.6:c.1314+4_1314+7del	ENSP00000400101.2:n.1314+4_1314+7del
ENST00000484495.5:n.464+4_464+7del
ENST00000490072.5:n.378+4_378+7del
NM_001160210.1:c.1314+4_1314+7del	NP_001153682.1:n.1314+4_1314+7del
NM_014251.2:c.1311+4_1311+7del	NP_055066.1:n.1311+4_1311+7del
NR_027662.1:n.1386+4_1386+7del
XM_006715831.2:c.1344+4_1344+7del	XP_006715894.1:n.1344+4_1344+7del
XM_011515727.1:c.1344+4_1344+7del	XP_011514029.1:n.1344+4_1344+7del
XM_011515728.1:c.459+4_459+7del	XP_011514030.1:n.459+4_459+7del
XM_006715831.4:c.1344+4_1344+7del	XP_006715894.1:n.1344+4_1344+7del
XM_011515727.3:c.1344+4_1344+7del	XP_011514029.1:n.1344+4_1344+7del
XM_017011663.1:c.1302+4_1302+7del	XP_016867152.1:n.1302+4_1302+7del
XM_017011664.2:c.459+4_459+7del	XP_016867153.1:n.459+4_459+7del
XM_017011665.1:c.459+4_459+7del	XP_016867154.1:n.459+4_459+7del
XR_001744525.2:n.1482+4_1482+7del
XR_002956405.1:n.2115+4_2115+7del
NM_014251.3:c.1311+4_1311+7del MANE Select	NP_055066.1:n.1311+4_1311+7del
NR_027662.2:n.1337+4_1337+7del
NM_001160210.2:c.1314+4_1314+7del	NP_001153682.1:n.1314+4_1314+7del