Canonical Allele Identifier: CA1727574813
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184100T= , CM000669.2:g.96184100T= GRCh38
NC_000007.13:g.95813412T= , CM000669.1:g.95813412T= GRCh37
NC_000007.12:g.95651348T= NCBI36
NG_012247.1:g.143048A=
NG_012247.2:g.143048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1177+177A= MANE Select ENSP00000265631.6:n.1177+177A=
ENST00000265631.9:c.1177+177A= ENSP00000265631.5:n.1177+177A=
ENST00000416240.6:c.1180+177A= ENSP00000400101.2:n.1180+177A=
ENST00000484495.5:n.330+177A=
ENST00000490072.5:n.244+177A=
ENST00000492869.1:n.298+177A=
NM_001160210.1:c.1180+177A= NP_001153682.1:n.1180+177A=
NM_014251.2:c.1177+177A= NP_055066.1:n.1177+177A=
NR_027662.1:n.1252+177A=
XM_006715831.2:c.1210+177A= XP_006715894.1:n.1210+177A=
XM_011515727.1:c.1210+177A= XP_011514029.1:n.1210+177A=
XM_011515728.1:c.325+177A= XP_011514030.1:n.325+177A=
XM_006715831.4:c.1210+177A= XP_006715894.1:n.1210+177A=
XM_011515727.3:c.1210+177A= XP_011514029.1:n.1210+177A=
XM_017011663.1:c.1168+177A= XP_016867152.1:n.1168+177A=
XM_017011664.2:c.325+177A= XP_016867153.1:n.325+177A=
XM_017011665.1:c.325+177A= XP_016867154.1:n.325+177A=
XR_001744525.2:n.1348+177A=
XR_002956405.1:n.1981+177A=
NM_014251.3:c.1177+177A= MANE Select NP_055066.1:n.1177+177A=
NR_027662.2:n.1203+177A=
NM_001160210.2:c.1180+177A= NP_001153682.1:n.1180+177A=