Canonical Allele Identifier: CA4353277

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96208898T>C , CM000669.2:g.96208898T>C	GRCh38
NC_000007.13:g.95838210T>C , CM000669.1:g.95838210T>C	GRCh37
NC_000007.12:g.95676146T>C	NCBI36
NG_012247.1:g.118250A>G
NG_012247.2:g.118250A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.408A>G MANE Select	NP_055066.1:p.Leu136=
ENST00000265631.10:c.408A>G MANE Select	ENSP00000265631.6:p.Leu136=
NM_001160210.1:c.408A>G	NP_001153682.1:p.Leu136=
NM_001160210.2:c.408A>G	NP_001153682.1:p.Leu136=
NM_014251.2:c.408A>G	NP_055066.1:p.Leu136=
NR_027662.1:n.483A>G
NR_027662.2:n.434A>G
ENST00000265631.9:c.408A>G	ENSP00000265631.5:p.Leu136=
ENST00000416240.6:c.408A>G	ENSP00000400101.2:p.Leu136=
ENST00000472162.2:c.*70A>G	ENSP00000473505.1:n.*70A>G
XM_006715831.2:c.441A>G	XP_006715894.1:p.Leu147=
XM_006715831.4:c.441A>G	XP_006715894.1:p.Leu147=
XM_011515727.1:c.441A>G	XP_011514029.1:p.Leu147=
XM_011515727.3:c.441A>G	XP_011514029.1:p.Leu147=
XM_017011663.1:c.399A>G	XP_016867152.1:p.Leu133=
XM_017011664.2:c.-351A>G	XP_016867153.1:n.-351A>G
XM_017011665.1:c.-351A>G	XP_016867154.1:n.-351A>G
XR_001744525.2:n.579A>G
XR_002956405.1:n.721A>G