Canonical Allele Identifier: CA1727580013

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189105_96189106delinsAT , CM000669.2:g.96189105_96189106delinsAT	GRCh38
NC_000007.13:g.95818417_95818418delinsAT , CM000669.1:g.95818417_95818418delinsAT	GRCh37
NC_000007.12:g.95656353_95656354delinsAT	NCBI36
NG_012247.1:g.138042_138043delinsAT
NG_012247.2:g.138042_138043delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.933+188_933+189delinsAT MANE Select	ENSP00000265631.6:n.933+188_933+189delinsAT
ENST00000265631.9:c.933+188_933+189delinsAT	ENSP00000265631.5:n.933+188_933+189delinsAT
ENST00000416240.6:c.933+188_933+189delinsAT	ENSP00000400101.2:n.933+188_933+189delinsAT
ENST00000484495.5:n.86+188_86+189delinsAT
NM_001160210.1:c.933+188_933+189delinsAT	NP_001153682.1:n.933+188_933+189delinsAT
NM_014251.2:c.933+188_933+189delinsAT	NP_055066.1:n.933+188_933+189delinsAT
NR_027662.1:n.1008+188_1008+189delinsAT
XM_006715831.2:c.966+188_966+189delinsAT	XP_006715894.1:n.966+188_966+189delinsAT
XM_011515727.1:c.966+188_966+189delinsAT	XP_011514029.1:n.966+188_966+189delinsAT
XM_011515728.1:c.81+188_81+189delinsAT	XP_011514030.1:n.81+188_81+189delinsAT
XM_006715831.4:c.966+188_966+189delinsAT	XP_006715894.1:n.966+188_966+189delinsAT
XM_011515727.3:c.966+188_966+189delinsAT	XP_011514029.1:n.966+188_966+189delinsAT
XM_017011663.1:c.924+188_924+189delinsAT	XP_016867152.1:n.924+188_924+189delinsAT
XM_017011664.2:c.81+188_81+189delinsAT	XP_016867153.1:n.81+188_81+189delinsAT
XM_017011665.1:c.81+188_81+189delinsAT	XP_016867154.1:n.81+188_81+189delinsAT
XR_001744525.2:n.1104+188_1104+189delinsAT
XR_002956405.1:n.1246+188_1246+189delinsAT
NM_014251.3:c.933+188_933+189delinsAT MANE Select	NP_055066.1:n.933+188_933+189delinsAT
NR_027662.2:n.959+188_959+189delinsAT
NM_001160210.2:c.933+188_933+189delinsAT	NP_001153682.1:n.933+188_933+189delinsAT