Canonical Allele Identifier: CA368262221

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818650C>T (hg19) ; chr7:g.96189338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189338C>T , CM000669.2:g.96189338C>T	GRCh38
NC_000007.13:g.95818650C>T , CM000669.1:g.95818650C>T	GRCh37
NC_000007.12:g.95656586C>T	NCBI36
NG_012247.1:g.137810G>A
NG_012247.2:g.137810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.889G>A MANE Select	ENSP00000265631.6:p.Glu297Lys
ENST00000265631.9:c.889G>A	ENSP00000265631.5:p.Glu297Lys
ENST00000416240.6:c.889G>A	ENSP00000400101.2:p.Glu297Lys
ENST00000484495.5:n.42G>A
NM_001160210.1:c.889G>A	NP_001153682.1:p.Glu297Lys
NM_014251.2:c.889G>A	NP_055066.1:p.Glu297Lys
NR_027662.1:n.964G>A
XM_006715831.2:c.922G>A	XP_006715894.1:p.Glu308Lys
XM_011515727.1:c.922G>A	XP_011514029.1:p.Glu308Lys
XM_011515728.1:c.37G>A	XP_011514030.1:p.Glu13Lys
XM_006715831.4:c.922G>A	XP_006715894.1:p.Glu308Lys
XM_011515727.3:c.922G>A	XP_011514029.1:p.Glu308Lys
XM_017011663.1:c.880G>A	XP_016867152.1:p.Glu294Lys
XM_017011664.2:c.37G>A	XP_016867153.1:p.Glu13Lys
XM_017011665.1:c.37G>A	XP_016867154.1:p.Glu13Lys
XR_001744525.2:n.1060G>A
XR_002956405.1:n.1202G>A
NM_014251.3:c.889G>A MANE Select	NP_055066.1:p.Glu297Lys
NR_027662.2:n.915G>A
NM_001160210.2:c.889G>A	NP_001153682.1:p.Glu297Lys