Canonical Allele Identifier: CA456510853

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818642T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189330T>C , CM000669.2:g.96189330T>C	GRCh38
NC_000007.13:g.95818642T>C , CM000669.1:g.95818642T>C	GRCh37
NC_000007.12:g.95656578T>C	NCBI36
NG_012247.1:g.137818A>G
NG_012247.2:g.137818A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.897A>G MANE Select	ENSP00000265631.6:p.Gly299=
ENST00000265631.9:c.897A>G	ENSP00000265631.5:p.Gly299=
ENST00000416240.6:c.897A>G	ENSP00000400101.2:p.Gly299=
ENST00000484495.5:n.50A>G
NM_001160210.1:c.897A>G	NP_001153682.1:p.Gly299=
NM_014251.2:c.897A>G	NP_055066.1:p.Gly299=
NR_027662.1:n.972A>G
XM_006715831.2:c.930A>G	XP_006715894.1:p.Gly310=
XM_011515727.1:c.930A>G	XP_011514029.1:p.Gly310=
XM_011515728.1:c.45A>G	XP_011514030.1:p.Gly15=
XM_006715831.4:c.930A>G	XP_006715894.1:p.Gly310=
XM_011515727.3:c.930A>G	XP_011514029.1:p.Gly310=
XM_017011663.1:c.888A>G	XP_016867152.1:p.Gly296=
XM_017011664.2:c.45A>G	XP_016867153.1:p.Gly15=
XM_017011665.1:c.45A>G	XP_016867154.1:p.Gly15=
XR_001744525.2:n.1068A>G
XR_002956405.1:n.1210A>G
NM_014251.3:c.897A>G MANE Select	NP_055066.1:p.Gly299=
NR_027662.2:n.923A>G
NM_001160210.2:c.897A>G	NP_001153682.1:p.Gly299=