Canonical Allele Identifier: CA368262156
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189328G>T , CM000669.2:g.96189328G>T GRCh38
NC_000007.13:g.95818640G>T , CM000669.1:g.95818640G>T GRCh37
NC_000007.12:g.95656576G>T NCBI36
NG_012247.1:g.137820C>A
NG_012247.2:g.137820C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.899C>A MANE Select ENSP00000265631.6:p.Thr300Asn
ENST00000265631.9:c.899C>A ENSP00000265631.5:p.Thr300Asn
ENST00000416240.6:c.899C>A ENSP00000400101.2:p.Thr300Asn
ENST00000484495.5:n.52C>A
NM_001160210.1:c.899C>A NP_001153682.1:p.Thr300Asn
NM_014251.2:c.899C>A NP_055066.1:p.Thr300Asn
NR_027662.1:n.974C>A
XM_006715831.2:c.932C>A XP_006715894.1:p.Thr311Asn
XM_011515727.1:c.932C>A XP_011514029.1:p.Thr311Asn
XM_011515728.1:c.47C>A XP_011514030.1:p.Thr16Asn
XM_006715831.4:c.932C>A XP_006715894.1:p.Thr311Asn
XM_011515727.3:c.932C>A XP_011514029.1:p.Thr311Asn
XM_017011663.1:c.890C>A XP_016867152.1:p.Thr297Asn
XM_017011664.2:c.47C>A XP_016867153.1:p.Thr16Asn
XM_017011665.1:c.47C>A XP_016867154.1:p.Thr16Asn
XR_001744525.2:n.1070C>A
XR_002956405.1:n.1212C>A
NM_014251.3:c.899C>A MANE Select NP_055066.1:p.Thr300Asn
NR_027662.2:n.925C>A
NM_001160210.2:c.899C>A NP_001153682.1:p.Thr300Asn