Canonical Allele Identifier: CA368262182
Gene: SLC25A13 HGNC NCBI

Linked Data

dbSNP Id: rs2116648305

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189333C>A , CM000669.2:g.96189333C>A GRCh38
NC_000007.13:g.95818645C>A , CM000669.1:g.95818645C>A GRCh37
NC_000007.12:g.95656581C>A NCBI36
NG_012247.1:g.137815G>T
NG_012247.2:g.137815G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.894G>T MANE Select ENSP00000265631.6:p.Glu298Asp
ENST00000265631.9:c.894G>T ENSP00000265631.5:p.Glu298Asp
ENST00000416240.6:c.894G>T ENSP00000400101.2:p.Glu298Asp
ENST00000484495.5:n.47G>T
NM_001160210.1:c.894G>T NP_001153682.1:p.Glu298Asp
NM_014251.2:c.894G>T NP_055066.1:p.Glu298Asp
NR_027662.1:n.969G>T
XM_006715831.2:c.927G>T XP_006715894.1:p.Glu309Asp
XM_011515727.1:c.927G>T XP_011514029.1:p.Glu309Asp
XM_011515728.1:c.42G>T XP_011514030.1:p.Glu14Asp
XM_006715831.4:c.927G>T XP_006715894.1:p.Glu309Asp
XM_011515727.3:c.927G>T XP_011514029.1:p.Glu309Asp
XM_017011663.1:c.885G>T XP_016867152.1:p.Glu295Asp
XM_017011664.2:c.42G>T XP_016867153.1:p.Glu14Asp
XM_017011665.1:c.42G>T XP_016867154.1:p.Glu14Asp
XR_001744525.2:n.1065G>T
XR_002956405.1:n.1207G>T
NM_014251.3:c.894G>T MANE Select NP_055066.1:p.Glu298Asp
NR_027662.2:n.920G>T
NM_001160210.2:c.894G>T NP_001153682.1:p.Glu298Asp