Canonical Allele Identifier: CA2683825457
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189427_96189433del , CM000669.2:g.96189427_96189433del GRCh38
NC_000007.13:g.95818739_95818745del , CM000669.1:g.95818739_95818745del GRCh37
NC_000007.12:g.95656675_95656681del NCBI36
NG_012247.1:g.137720_137726del
NG_012247.2:g.137720_137726del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.849-50_849-44del MANE Select ENSP00000265631.6:n.849-50_849-44del
ENST00000265631.9:c.849-50_849-44del ENSP00000265631.5:n.849-50_849-44del
ENST00000416240.6:c.849-50_849-44del ENSP00000400101.2:n.849-50_849-44del
NM_001160210.1:c.849-50_849-44del NP_001153682.1:n.849-50_849-44del
NM_014251.2:c.849-50_849-44del NP_055066.1:n.849-50_849-44del
NR_027662.1:n.924-50_924-44del
XM_006715831.2:c.882-50_882-44del XP_006715894.1:n.882-50_882-44del
XM_011515727.1:c.882-50_882-44del XP_011514029.1:n.882-50_882-44del
XM_011515728.1:c.-4-50_-4-44del XP_011514030.1:n.-4-50_-4-44del
XM_006715831.4:c.882-50_882-44del XP_006715894.1:n.882-50_882-44del
XM_011515727.3:c.882-50_882-44del XP_011514029.1:n.882-50_882-44del
XM_017011663.1:c.840-50_840-44del XP_016867152.1:n.840-50_840-44del
XM_017011664.2:c.-4-50_-4-44del XP_016867153.1:n.-4-50_-4-44del
XM_017011665.1:c.-4-50_-4-44del XP_016867154.1:n.-4-50_-4-44del
XR_001744525.2:n.1020-50_1020-44del
XR_002956405.1:n.1162-50_1162-44del
NM_014251.3:c.849-50_849-44del MANE Select NP_055066.1:n.849-50_849-44del
NR_027662.2:n.875-50_875-44del
NM_001160210.2:c.849-50_849-44del NP_001153682.1:n.849-50_849-44del