Canonical Allele Identifier: CA368262211
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189337T>C , CM000669.2:g.96189337T>C GRCh38
NC_000007.13:g.95818649T>C , CM000669.1:g.95818649T>C GRCh37
NC_000007.12:g.95656585T>C NCBI36
NG_012247.1:g.137811A>G
NG_012247.2:g.137811A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.890A>G MANE Select ENSP00000265631.6:p.Glu297Gly
ENST00000265631.9:c.890A>G ENSP00000265631.5:p.Glu297Gly
ENST00000416240.6:c.890A>G ENSP00000400101.2:p.Glu297Gly
ENST00000484495.5:n.43A>G
NM_001160210.1:c.890A>G NP_001153682.1:p.Glu297Gly
NM_014251.2:c.890A>G NP_055066.1:p.Glu297Gly
NR_027662.1:n.965A>G
XM_006715831.2:c.923A>G XP_006715894.1:p.Glu308Gly
XM_011515727.1:c.923A>G XP_011514029.1:p.Glu308Gly
XM_011515728.1:c.38A>G XP_011514030.1:p.Glu13Gly
XM_006715831.4:c.923A>G XP_006715894.1:p.Glu308Gly
XM_011515727.3:c.923A>G XP_011514029.1:p.Glu308Gly
XM_017011663.1:c.881A>G XP_016867152.1:p.Glu294Gly
XM_017011664.2:c.38A>G XP_016867153.1:p.Glu13Gly
XM_017011665.1:c.38A>G XP_016867154.1:p.Glu13Gly
XR_001744525.2:n.1061A>G
XR_002956405.1:n.1203A>G
NM_014251.3:c.890A>G MANE Select NP_055066.1:p.Glu297Gly
NR_027662.2:n.916A>G
NM_001160210.2:c.890A>G NP_001153682.1:p.Glu297Gly