Canonical Allele Identifier: CA456510881

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818681G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189369G>T , CM000669.2:g.96189369G>T	GRCh38
NC_000007.13:g.95818681G>T , CM000669.1:g.95818681G>T	GRCh37
NC_000007.12:g.95656617G>T	NCBI36
NG_012247.1:g.137779C>A
NG_012247.2:g.137779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.858C>A MANE Select	ENSP00000265631.6:p.Thr286=
ENST00000265631.9:c.858C>A	ENSP00000265631.5:p.Thr286=
ENST00000416240.6:c.858C>A	ENSP00000400101.2:p.Thr286=
ENST00000484495.5:n.11C>A
NM_001160210.1:c.858C>A	NP_001153682.1:p.Thr286=
NM_014251.2:c.858C>A	NP_055066.1:p.Thr286=
NR_027662.1:n.933C>A
XM_006715831.2:c.891C>A	XP_006715894.1:p.Thr297=
XM_011515727.1:c.891C>A	XP_011514029.1:p.Thr297=
XM_011515728.1:c.6C>A	XP_011514030.1:p.Thr2=
XM_006715831.4:c.891C>A	XP_006715894.1:p.Thr297=
XM_011515727.3:c.891C>A	XP_011514029.1:p.Thr297=
XM_017011663.1:c.849C>A	XP_016867152.1:p.Thr283=
XM_017011664.2:c.6C>A	XP_016867153.1:p.Thr2=
XM_017011665.1:c.6C>A	XP_016867154.1:p.Thr2=
XR_001744525.2:n.1029C>A
XR_002956405.1:n.1171C>A
NM_014251.3:c.858C>A MANE Select	NP_055066.1:p.Thr286=
NR_027662.2:n.884C>A
NM_001160210.2:c.858C>A	NP_001153682.1:p.Thr286=