Canonical Allele Identifier: CA368258339
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121940A>T , CM000669.2:g.96121940A>T GRCh38
NC_000007.13:g.95751252A>T , CM000669.1:g.95751252A>T GRCh37
NC_000007.12:g.95589188A>T NCBI36
NG_012247.1:g.205208T>A
NG_012247.2:g.205208T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1649T>A MANE Select ENSP00000265631.6:p.Val550Glu
ENST00000265631.9:c.1649T>A ENSP00000265631.5:p.Val550Glu
ENST00000416240.6:c.1652T>A ENSP00000400101.2:p.Val551Glu
ENST00000494085.1:n.59T>A
NM_001160210.1:c.1652T>A NP_001153682.1:p.Val551Glu
NM_014251.2:c.1649T>A NP_055066.1:p.Val550Glu
NR_027662.1:n.1724T>A
XM_006715831.2:c.1682T>A XP_006715894.1:p.Val561Glu
XM_011515728.1:c.797T>A XP_011514030.1:p.Val266Glu
XM_006715831.4:c.1682T>A XP_006715894.1:p.Val561Glu
XM_017011663.1:c.1640T>A XP_016867152.1:p.Val547Glu
XM_017011664.2:c.797T>A XP_016867153.1:p.Val266Glu
XM_017011665.1:c.797T>A XP_016867154.1:p.Val266Glu
XR_001744525.2:n.1895T>A
XR_002956405.1:n.2453T>A
NM_014251.3:c.1649T>A MANE Select NP_055066.1:p.Val550Glu
NR_027662.2:n.1675T>A
NM_001160210.2:c.1652T>A NP_001153682.1:p.Val551Glu