Canonical Allele Identifier: CA2514478102
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184260_96184289del , CM000669.2:g.96184260_96184289del GRCh38
NC_000007.13:g.95813572_95813601del , CM000669.1:g.95813572_95813601del GRCh37
NC_000007.12:g.95651508_95651537del NCBI36
NG_012247.1:g.142859_142888del
NG_012247.2:g.142859_142888del

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1165_1177+17del
ENST00000265631.9:c.1165_1177+17del
ENST00000416240.6:c.1168_1180+17del
ENST00000484495.5:n.318_330+17del
ENST00000490072.5:n.232_244+17del
ENST00000492869.1:n.286_298+17del
NM_001160210.1:c.1168_1180+17del
NM_014251.2:c.1165_1177+17del
NR_027662.1:n.1240_1252+17del
XM_006715831.2:c.1198_1210+17del
XM_011515727.1:c.1198_1210+17del
XM_011515728.1:c.313_325+17del
XM_006715831.4:c.1198_1210+17del
XM_011515727.3:c.1198_1210+17del
XM_017011663.1:c.1156_1168+17del
XM_017011664.2:c.313_325+17del
XM_017011665.1:c.313_325+17del
XR_001744525.2:n.1336_1348+17del
XR_002956405.1:n.1969_1981+17del
NM_014251.3:c.1165_1177+17del
NR_027662.2:n.1191_1203+17del
NM_001160210.2:c.1168_1180+17del