Canonical Allele Identifier: CA1727575000
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184286G= , CM000669.2:g.96184286G= GRCh38
NC_000007.13:g.95813598G= , CM000669.1:g.95813598G= GRCh37
NC_000007.12:g.95651534G= NCBI36
NG_012247.1:g.142862C=
NG_012247.2:g.142862C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1168C= MANE Select ENSP00000265631.6:p.Leu390=
ENST00000265631.9:c.1168C= ENSP00000265631.5:p.Leu390=
ENST00000416240.6:c.1171C= ENSP00000400101.2:p.Leu391=
ENST00000484495.5:n.321C=
ENST00000490072.5:n.235C=
ENST00000492869.1:n.289C=
NM_001160210.1:c.1171C= NP_001153682.1:p.Leu391=
NM_014251.2:c.1168C= NP_055066.1:p.Leu390=
NR_027662.1:n.1243C=
XM_006715831.2:c.1201C= XP_006715894.1:p.Leu401=
XM_011515727.1:c.1201C= XP_011514029.1:p.Leu401=
XM_011515728.1:c.316C= XP_011514030.1:p.Leu106=
XM_006715831.4:c.1201C= XP_006715894.1:p.Leu401=
XM_011515727.3:c.1201C= XP_011514029.1:p.Leu401=
XM_017011663.1:c.1159C= XP_016867152.1:p.Leu387=
XM_017011664.2:c.316C= XP_016867153.1:p.Leu106=
XM_017011665.1:c.316C= XP_016867154.1:p.Leu106=
XR_001744525.2:n.1339C=
XR_002956405.1:n.1972C=
NM_014251.3:c.1168C= MANE Select NP_055066.1:p.Leu390=
NR_027662.2:n.1194C=
NM_001160210.2:c.1171C= NP_001153682.1:p.Leu391=