Canonical Allele Identifier: CA1727517389
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121392_96121394delinsAAC , CM000669.2:g.96121392_96121394delinsAAC GRCh38
NC_000007.13:g.95750704_95750706delinsAAC , CM000669.1:g.95750704_95750706delinsAAC GRCh37
NC_000007.12:g.95588640_95588642delinsAAC NCBI36
NG_012247.1:g.205754_205756delinsGTT
NG_012247.2:g.205754_205756delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1842-17_1842-15delinsGTT MANE Select ENSP00000265631.6:n.1842-17_1842-15delinsGTT
ENST00000265631.9:c.1842-17_1842-15delinsGTT ENSP00000265631.5:n.1842-17_1842-15delinsGTT
ENST00000416240.6:c.1845-17_1845-15delinsGTT ENSP00000400101.2:n.1845-17_1845-15delinsGTT
ENST00000494085.1:n.345-17_345-15delinsGTT
NM_001160210.1:c.1845-17_1845-15delinsGTT NP_001153682.1:n.1845-17_1845-15delinsGTT
NM_014251.2:c.1842-17_1842-15delinsGTT NP_055066.1:n.1842-17_1842-15delinsGTT
NR_027662.1:n.1917-17_1917-15delinsGTT
XM_006715831.2:c.1875-17_1875-15delinsGTT XP_006715894.1:n.1875-17_1875-15delinsGTT
XM_011515728.1:c.990-17_990-15delinsGTT XP_011514030.1:n.990-17_990-15delinsGTT
XM_006715831.4:c.1875-17_1875-15delinsGTT XP_006715894.1:n.1875-17_1875-15delinsGTT
XM_017011663.1:c.1833-17_1833-15delinsGTT XP_016867152.1:n.1833-17_1833-15delinsGTT
XM_017011664.2:c.990-17_990-15delinsGTT XP_016867153.1:n.990-17_990-15delinsGTT
XM_017011665.1:c.990-17_990-15delinsGTT XP_016867154.1:n.990-17_990-15delinsGTT
XR_001744525.2:n.2088-17_2088-15delinsGTT
XR_002956405.1:n.2646-17_2646-15delinsGTT
NM_014251.3:c.1842-17_1842-15delinsGTT MANE Select NP_055066.1:n.1842-17_1842-15delinsGTT
NR_027662.2:n.1868-17_1868-15delinsGTT
NM_001160210.2:c.1845-17_1845-15delinsGTT NP_001153682.1:n.1845-17_1845-15delinsGTT