Canonical Allele Identifier: CA2695208127

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96170036_96170045del , CM000669.2:g.96170036_96170045del	GRCh38
NC_000007.13:g.95799348_95799357del , CM000669.1:g.95799348_95799357del	GRCh37
NC_000007.12:g.95637284_95637293del	NCBI36
NG_012247.1:g.157103_157112del
NG_012247.2:g.157103_157112del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1311_1311+9del
ENST00000265631.9:c.1311_1311+9del
ENST00000416240.6:c.1314_1314+9del
ENST00000484495.5:n.464_464+9del
ENST00000490072.5:n.378_378+9del
NM_001160210.1:c.1314_1314+9del
NM_014251.2:c.1311_1311+9del
NR_027662.1:n.1386_1386+9del
XM_006715831.2:c.1344_1344+9del
XM_011515727.1:c.1344_1344+9del
XM_011515728.1:c.459_459+9del
XM_006715831.4:c.1344_1344+9del
XM_011515727.3:c.1344_1344+9del
XM_017011663.1:c.1302_1302+9del
XM_017011664.2:c.459_459+9del
XM_017011665.1:c.459_459+9del
XR_001744525.2:n.1482_1482+9del
XR_002956405.1:n.2115_2115+9del
NM_014251.3:c.1311_1311+9del
NR_027662.2:n.1337_1337+9del
NM_001160210.2:c.1314_1314+9del