Canonical Allele Identifier: CA368258013
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121854A>G , CM000669.2:g.96121854A>G GRCh38
NC_000007.13:g.95751166A>G , CM000669.1:g.95751166A>G GRCh37
NC_000007.12:g.95589102A>G NCBI36
NG_012247.1:g.205294T>C
NG_012247.2:g.205294T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1735T>C MANE Select ENSP00000265631.6:p.Trp579Arg
ENST00000265631.9:c.1735T>C ENSP00000265631.5:p.Trp579Arg
ENST00000416240.6:c.1738T>C ENSP00000400101.2:p.Trp580Arg
ENST00000494085.1:n.145T>C
NM_001160210.1:c.1738T>C NP_001153682.1:p.Trp580Arg
NM_014251.2:c.1735T>C NP_055066.1:p.Trp579Arg
NR_027662.1:n.1810T>C
XM_006715831.2:c.1768T>C XP_006715894.1:p.Trp590Arg
XM_011515728.1:c.883T>C XP_011514030.1:p.Trp295Arg
XM_006715831.4:c.1768T>C XP_006715894.1:p.Trp590Arg
XM_017011663.1:c.1726T>C XP_016867152.1:p.Trp576Arg
XM_017011664.2:c.883T>C XP_016867153.1:p.Trp295Arg
XM_017011665.1:c.883T>C XP_016867154.1:p.Trp295Arg
XR_001744525.2:n.1981T>C
XR_002956405.1:n.2539T>C
NM_014251.3:c.1735T>C MANE Select NP_055066.1:p.Trp579Arg
NR_027662.2:n.1761T>C
NM_001160210.2:c.1738T>C NP_001153682.1:p.Trp580Arg