Canonical Allele Identifier: CA1727517135

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121234_96121236delinsTTG , CM000669.2:g.96121234_96121236delinsTTG	GRCh38
NC_000007.13:g.95750546_95750548delinsTTG , CM000669.1:g.95750546_95750548delinsTTG	GRCh37
NC_000007.12:g.95588482_95588484delinsTTG	NCBI36
NG_012247.1:g.205912_205914delinsCAA
NG_012247.2:g.205912_205914delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1983_1985delinsCAA MANE Select	ENSP00000265631.6:p.Phe661=
ENST00000265631.9:c.1983_1985delinsCAA	ENSP00000265631.5:p.Phe661=
ENST00000416240.6:c.1986_1988delinsCAA	ENSP00000400101.2:p.Phe662=
ENST00000494085.1:n.486_488delinsCAA
NM_001160210.1:c.1986_1988delinsCAA	NP_001153682.1:p.Phe662=
NM_014251.2:c.1983_1985delinsCAA	NP_055066.1:p.Phe661=
NR_027662.1:n.2058_2060delinsCAA
XM_006715831.2:c.2016_2018delinsCAA	XP_006715894.1:p.Phe672=
XM_011515728.1:c.1131_1133delinsCAA	XP_011514030.1:p.Phe377=
XM_006715831.4:c.2016_2018delinsCAA	XP_006715894.1:p.Phe672=
XM_017011663.1:c.1974_1976delinsCAA	XP_016867152.1:p.Phe658=
XM_017011664.2:c.1131_1133delinsCAA	XP_016867153.1:p.Phe377=
XM_017011665.1:c.1131_1133delinsCAA	XP_016867154.1:p.Phe377=
XR_001744525.2:n.2229_2231delinsCAA
XR_002956405.1:n.2787_2789delinsCAA
NM_014251.3:c.1983_1985delinsCAA MANE Select	NP_055066.1:p.Phe661=
NR_027662.2:n.2009_2011delinsCAA
NM_001160210.2:c.1986_1988delinsCAA	NP_001153682.1:p.Phe662=