Canonical Allele Identifier: CA1104707160
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189469_96189470del , CM000669.2:g.96189469_96189470del GRCh38
NC_000007.13:g.95818781_95818782del , CM000669.1:g.95818781_95818782del GRCh37
NC_000007.12:g.95656717_95656718del NCBI36
NG_012247.1:g.137678_137679del
NG_012247.2:g.137678_137679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.849-92_849-91del MANE Select ENSP00000265631.6:n.849-92_849-91del
ENST00000265631.9:c.849-92_849-91del ENSP00000265631.5:n.849-92_849-91del
ENST00000416240.6:c.849-92_849-91del ENSP00000400101.2:n.849-92_849-91del
NM_001160210.1:c.849-92_849-91del NP_001153682.1:n.849-92_849-91del
NM_014251.2:c.849-92_849-91del NP_055066.1:n.849-92_849-91del
NR_027662.1:n.924-92_924-91del
XM_006715831.2:c.882-92_882-91del XP_006715894.1:n.882-92_882-91del
XM_011515727.1:c.882-92_882-91del XP_011514029.1:n.882-92_882-91del
XM_011515728.1:c.-4-92_-4-91del XP_011514030.1:n.-4-92_-4-91del
XM_006715831.4:c.882-92_882-91del XP_006715894.1:n.882-92_882-91del
XM_011515727.3:c.882-92_882-91del XP_011514029.1:n.882-92_882-91del
XM_017011663.1:c.840-92_840-91del XP_016867152.1:n.840-92_840-91del
XM_017011664.2:c.-4-92_-4-91del XP_016867153.1:n.-4-92_-4-91del
XM_017011665.1:c.-4-92_-4-91del XP_016867154.1:n.-4-92_-4-91del
XR_001744525.2:n.1020-92_1020-91del
XR_002956405.1:n.1162-92_1162-91del
NM_014251.3:c.849-92_849-91del MANE Select NP_055066.1:n.849-92_849-91del
NR_027662.2:n.875-92_875-91del
NM_001160210.2:c.849-92_849-91del NP_001153682.1:n.849-92_849-91del