Canonical Allele Identifier: CA1104712042
Gene: SLC25A13 HGNC NCBI

Linked Data

dbSNP Id: rs1794535552

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184276_96184277del , CM000669.2:g.96184276_96184277del GRCh38
NC_000007.13:g.95813588_95813589del , CM000669.1:g.95813588_95813589del GRCh37
NC_000007.12:g.95651524_95651525del NCBI36
NG_012247.1:g.142871_142872del
NG_012247.2:g.142871_142872del

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1177_1177+1del
ENST00000265631.9:c.1177_1177+1del
ENST00000416240.6:c.1180_1180+1del
ENST00000484495.5:n.330_330+1del
ENST00000490072.5:n.244_244+1del
ENST00000492869.1:n.298_298+1del
NM_001160210.1:c.1180_1180+1del
NM_014251.2:c.1177_1177+1del
NR_027662.1:n.1252_1252+1del
XM_006715831.2:c.1210_1210+1del
XM_011515727.1:c.1210_1210+1del
XM_011515728.1:c.325_325+1del
XM_006715831.4:c.1210_1210+1del
XM_011515727.3:c.1210_1210+1del
XM_017011663.1:c.1168_1168+1del
XM_017011664.2:c.325_325+1del
XM_017011665.1:c.325_325+1del
XR_001744525.2:n.1348_1348+1del
XR_002956405.1:n.1981_1981+1del
NM_014251.3:c.1177_1177+1del
NR_027662.2:n.1203_1203+1del
NM_001160210.2:c.1180_1180+1del