Canonical Allele Identifier: CA1727517416

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121410_96121411delinsAT , CM000669.2:g.96121410_96121411delinsAT	GRCh38
NC_000007.13:g.95750722_95750723delinsAT , CM000669.1:g.95750722_95750723delinsAT	GRCh37
NC_000007.12:g.95588658_95588659delinsAT	NCBI36
NG_012247.1:g.205737_205738delinsAT
NG_012247.2:g.205737_205738delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-34_1842-33delinsAT MANE Select	ENSP00000265631.6:n.1842-34_1842-33delinsAT
ENST00000265631.9:c.1842-34_1842-33delinsAT	ENSP00000265631.5:n.1842-34_1842-33delinsAT
ENST00000416240.6:c.1845-34_1845-33delinsAT	ENSP00000400101.2:n.1845-34_1845-33delinsAT
ENST00000494085.1:n.345-34_345-33delinsAT
NM_001160210.1:c.1845-34_1845-33delinsAT	NP_001153682.1:n.1845-34_1845-33delinsAT
NM_014251.2:c.1842-34_1842-33delinsAT	NP_055066.1:n.1842-34_1842-33delinsAT
NR_027662.1:n.1917-34_1917-33delinsAT
XM_006715831.2:c.1875-34_1875-33delinsAT	XP_006715894.1:n.1875-34_1875-33delinsAT
XM_011515728.1:c.990-34_990-33delinsAT	XP_011514030.1:n.990-34_990-33delinsAT
XM_006715831.4:c.1875-34_1875-33delinsAT	XP_006715894.1:n.1875-34_1875-33delinsAT
XM_017011663.1:c.1833-34_1833-33delinsAT	XP_016867152.1:n.1833-34_1833-33delinsAT
XM_017011664.2:c.990-34_990-33delinsAT	XP_016867153.1:n.990-34_990-33delinsAT
XM_017011665.1:c.990-34_990-33delinsAT	XP_016867154.1:n.990-34_990-33delinsAT
XR_001744525.2:n.2088-34_2088-33delinsAT
XR_002956405.1:n.2646-34_2646-33delinsAT
NM_014251.3:c.1842-34_1842-33delinsAT MANE Select	NP_055066.1:n.1842-34_1842-33delinsAT
NR_027662.2:n.1868-34_1868-33delinsAT
NM_001160210.2:c.1845-34_1845-33delinsAT	NP_001153682.1:n.1845-34_1845-33delinsAT