Canonical Allele Identifier: CA1727580544
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189548_96189552delinsATTCC , CM000669.2:g.96189548_96189552delinsATTCC GRCh38
NC_000007.13:g.95818860_95818864delinsATTCC , CM000669.1:g.95818860_95818864delinsATTCC GRCh37
NC_000007.12:g.95656796_95656800delinsATTCC NCBI36
NG_012247.1:g.137596_137600delinsGGAAT
NG_012247.2:g.137596_137600delinsGGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.848+29_848+33delinsGGAAT MANE Select ENSP00000265631.6:n.848+29_848+33delinsGGAAT
ENST00000265631.9:c.848+29_848+33delinsGGAAT ENSP00000265631.5:n.848+29_848+33delinsGGAAT
ENST00000416240.6:c.848+29_848+33delinsGGAAT ENSP00000400101.2:n.848+29_848+33delinsGGAAT
NM_001160210.1:c.848+29_848+33delinsGGAAT NP_001153682.1:n.848+29_848+33delinsGGAAT
NM_014251.2:c.848+29_848+33delinsGGAAT NP_055066.1:n.848+29_848+33delinsGGAAT
NR_027662.1:n.923+29_923+33delinsGGAAT
XM_006715831.2:c.881+29_881+33delinsGGAAT XP_006715894.1:n.881+29_881+33delinsGGAAT
XM_011515727.1:c.881+29_881+33delinsGGAAT XP_011514029.1:n.881+29_881+33delinsGGAAT
XM_011515728.1:c.-4-174_-4-170delinsGGAAT XP_011514030.1:n.-4-174_-4-170delinsGGAAT
XM_006715831.4:c.881+29_881+33delinsGGAAT XP_006715894.1:n.881+29_881+33delinsGGAAT
XM_011515727.3:c.881+29_881+33delinsGGAAT XP_011514029.1:n.881+29_881+33delinsGGAAT
XM_017011663.1:c.839+29_839+33delinsGGAAT XP_016867152.1:n.839+29_839+33delinsGGAAT
XM_017011664.2:c.-4-174_-4-170delinsGGAAT XP_016867153.1:n.-4-174_-4-170delinsGGAAT
XM_017011665.1:c.-4-174_-4-170delinsGGAAT XP_016867154.1:n.-4-174_-4-170delinsGGAAT
XR_001744525.2:n.1019+29_1019+33delinsGGAAT
XR_002956405.1:n.1161+29_1161+33delinsGGAAT
NM_014251.3:c.848+29_848+33delinsGGAAT MANE Select NP_055066.1:n.848+29_848+33delinsGGAAT
NR_027662.2:n.874+29_874+33delinsGGAAT
NM_001160210.2:c.848+29_848+33delinsGGAAT NP_001153682.1:n.848+29_848+33delinsGGAAT