Canonical Allele Identifier: CA1104707154
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189462_96189463del , CM000669.2:g.96189462_96189463del GRCh38
NC_000007.13:g.95818774_95818775del , CM000669.1:g.95818774_95818775del GRCh37
NC_000007.12:g.95656710_95656711del NCBI36
NG_012247.1:g.137685_137686del
NG_012247.2:g.137685_137686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.849-85_849-84del MANE Select ENSP00000265631.6:n.849-85_849-84del
ENST00000265631.9:c.849-85_849-84del ENSP00000265631.5:n.849-85_849-84del
ENST00000416240.6:c.849-85_849-84del ENSP00000400101.2:n.849-85_849-84del
NM_001160210.1:c.849-85_849-84del NP_001153682.1:n.849-85_849-84del
NM_014251.2:c.849-85_849-84del NP_055066.1:n.849-85_849-84del
NR_027662.1:n.924-85_924-84del
XM_006715831.2:c.882-85_882-84del XP_006715894.1:n.882-85_882-84del
XM_011515727.1:c.882-85_882-84del XP_011514029.1:n.882-85_882-84del
XM_011515728.1:c.-4-85_-4-84del XP_011514030.1:n.-4-85_-4-84del
XM_006715831.4:c.882-85_882-84del XP_006715894.1:n.882-85_882-84del
XM_011515727.3:c.882-85_882-84del XP_011514029.1:n.882-85_882-84del
XM_017011663.1:c.840-85_840-84del XP_016867152.1:n.840-85_840-84del
XM_017011664.2:c.-4-85_-4-84del XP_016867153.1:n.-4-85_-4-84del
XM_017011665.1:c.-4-85_-4-84del XP_016867154.1:n.-4-85_-4-84del
XR_001744525.2:n.1020-85_1020-84del
XR_002956405.1:n.1162-85_1162-84del
NM_014251.3:c.849-85_849-84del MANE Select NP_055066.1:n.849-85_849-84del
NR_027662.2:n.875-85_875-84del
NM_001160210.2:c.849-85_849-84del NP_001153682.1:n.849-85_849-84del