Canonical Allele Identifier: CA456510830

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818612C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189300C>T , CM000669.2:g.96189300C>T	GRCh38
NC_000007.13:g.95818612C>T , CM000669.1:g.95818612C>T	GRCh37
NC_000007.12:g.95656548C>T	NCBI36
NG_012247.1:g.137848G>A
NG_012247.2:g.137848G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.927G>A MANE Select	ENSP00000265631.6:p.Gln309=
ENST00000265631.9:c.927G>A	ENSP00000265631.5:p.Gln309=
ENST00000416240.6:c.927G>A	ENSP00000400101.2:p.Gln309=
ENST00000484495.5:n.80G>A
NM_001160210.1:c.927G>A	NP_001153682.1:p.Gln309=
NM_014251.2:c.927G>A	NP_055066.1:p.Gln309=
NR_027662.1:n.1002G>A
XM_006715831.2:c.960G>A	XP_006715894.1:p.Gln320=
XM_011515727.1:c.960G>A	XP_011514029.1:p.Gln320=
XM_011515728.1:c.75G>A	XP_011514030.1:p.Gln25=
XM_006715831.4:c.960G>A	XP_006715894.1:p.Gln320=
XM_011515727.3:c.960G>A	XP_011514029.1:p.Gln320=
XM_017011663.1:c.918G>A	XP_016867152.1:p.Gln306=
XM_017011664.2:c.75G>A	XP_016867153.1:p.Gln25=
XM_017011665.1:c.75G>A	XP_016867154.1:p.Gln25=
XR_001744525.2:n.1098G>A
XR_002956405.1:n.1240G>A
NM_014251.3:c.927G>A MANE Select	NP_055066.1:p.Gln309=
NR_027662.2:n.953G>A
NM_001160210.2:c.927G>A	NP_001153682.1:p.Gln309=