Canonical Allele Identifier: CA1727574834
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184122G= , CM000669.2:g.96184122G= GRCh38
NC_000007.13:g.95813434G= , CM000669.1:g.95813434G= GRCh37
NC_000007.12:g.95651370G= NCBI36
NG_012247.1:g.143026C=
NG_012247.2:g.143026C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1177+155C= MANE Select ENSP00000265631.6:n.1177+155C=
ENST00000265631.9:c.1177+155C= ENSP00000265631.5:n.1177+155C=
ENST00000416240.6:c.1180+155C= ENSP00000400101.2:n.1180+155C=
ENST00000484495.5:n.330+155C=
ENST00000490072.5:n.244+155C=
ENST00000492869.1:n.298+155C=
NM_001160210.1:c.1180+155C= NP_001153682.1:n.1180+155C=
NM_014251.2:c.1177+155C= NP_055066.1:n.1177+155C=
NR_027662.1:n.1252+155C=
XM_006715831.2:c.1210+155C= XP_006715894.1:n.1210+155C=
XM_011515727.1:c.1210+155C= XP_011514029.1:n.1210+155C=
XM_011515728.1:c.325+155C= XP_011514030.1:n.325+155C=
XM_006715831.4:c.1210+155C= XP_006715894.1:n.1210+155C=
XM_011515727.3:c.1210+155C= XP_011514029.1:n.1210+155C=
XM_017011663.1:c.1168+155C= XP_016867152.1:n.1168+155C=
XM_017011664.2:c.325+155C= XP_016867153.1:n.325+155C=
XM_017011665.1:c.325+155C= XP_016867154.1:n.325+155C=
XR_001744525.2:n.1348+155C=
XR_002956405.1:n.1981+155C=
NM_014251.3:c.1177+155C= MANE Select NP_055066.1:n.1177+155C=
NR_027662.2:n.1203+155C=
NM_001160210.2:c.1180+155C= NP_001153682.1:n.1180+155C=