Canonical Allele Identifier: CA368258430

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96170053-C-T
• MyVariant Identifiers: chr7:g.95799365C>T (hg19) ; chr7:g.96170053C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96170053C>T , CM000669.2:g.96170053C>T	GRCh38
NC_000007.13:g.95799365C>T , CM000669.1:g.95799365C>T	GRCh37
NC_000007.12:g.95637301C>T	NCBI36
NG_012247.1:g.157095G>A
NG_012247.2:g.157095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1303G>A MANE Select	ENSP00000265631.6:p.Gly435Arg
ENST00000265631.9:c.1303G>A	ENSP00000265631.5:p.Gly435Arg
ENST00000416240.6:c.1306G>A	ENSP00000400101.2:p.Gly436Arg
ENST00000484495.5:n.456G>A
ENST00000490072.5:n.370G>A
ENST00000492869.1:n.424G>A
NM_001160210.1:c.1306G>A	NP_001153682.1:p.Gly436Arg
NM_014251.2:c.1303G>A	NP_055066.1:p.Gly435Arg
NR_027662.1:n.1378G>A
XM_006715831.2:c.1336G>A	XP_006715894.1:p.Gly446Arg
XM_011515727.1:c.1336G>A	XP_011514029.1:p.Gly446Arg
XM_011515728.1:c.451G>A	XP_011514030.1:p.Gly151Arg
XM_006715831.4:c.1336G>A	XP_006715894.1:p.Gly446Arg
XM_011515727.3:c.1336G>A	XP_011514029.1:p.Gly446Arg
XM_017011663.1:c.1294G>A	XP_016867152.1:p.Gly432Arg
XM_017011664.2:c.451G>A	XP_016867153.1:p.Gly151Arg
XM_017011665.1:c.451G>A	XP_016867154.1:p.Gly151Arg
XR_001744525.2:n.1474G>A
XR_002956405.1:n.2107G>A
NM_014251.3:c.1303G>A MANE Select	NP_055066.1:p.Gly435Arg
NR_027662.2:n.1329G>A
NM_001160210.2:c.1306G>A	NP_001153682.1:p.Gly436Arg