Canonical Allele Identifier: CA1727574984
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184284C= , CM000669.2:g.96184284C= GRCh38
NC_000007.13:g.95813596C= , CM000669.1:g.95813596C= GRCh37
NC_000007.12:g.95651532C= NCBI36
NG_012247.1:g.142864G=
NG_012247.2:g.142864G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1170G= MANE Select ENSP00000265631.6:p.Leu390=
ENST00000265631.9:c.1170G= ENSP00000265631.5:p.Leu390=
ENST00000416240.6:c.1173G= ENSP00000400101.2:p.Leu391=
ENST00000484495.5:n.323G=
ENST00000490072.5:n.237G=
ENST00000492869.1:n.291G=
NM_001160210.1:c.1173G= NP_001153682.1:p.Leu391=
NM_014251.2:c.1170G= NP_055066.1:p.Leu390=
NR_027662.1:n.1245G=
XM_006715831.2:c.1203G= XP_006715894.1:p.Leu401=
XM_011515727.1:c.1203G= XP_011514029.1:p.Leu401=
XM_011515728.1:c.318G= XP_011514030.1:p.Leu106=
XM_006715831.4:c.1203G= XP_006715894.1:p.Leu401=
XM_011515727.3:c.1203G= XP_011514029.1:p.Leu401=
XM_017011663.1:c.1161G= XP_016867152.1:p.Leu387=
XM_017011664.2:c.318G= XP_016867153.1:p.Leu106=
XM_017011665.1:c.318G= XP_016867154.1:p.Leu106=
XR_001744525.2:n.1341G=
XR_002956405.1:n.1974G=
NM_014251.3:c.1170G= MANE Select NP_055066.1:p.Leu390=
NR_027662.2:n.1196G=
NM_001160210.2:c.1173G= NP_001153682.1:p.Leu391=