Canonical Allele Identifier: CA368256943

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121201-C-G
• MyVariant Identifiers: chr7:g.95750513C>G (hg19) ; chr7:g.96121201C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121201C>G , CM000669.2:g.96121201C>G	GRCh38
NC_000007.13:g.95750513C>G , CM000669.1:g.95750513C>G	GRCh37
NC_000007.12:g.95588449C>G	NCBI36
NG_012247.1:g.205947G>C
NG_012247.2:g.205947G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.2018G>C MANE Select	ENSP00000265631.6:p.Gly673Ala
ENST00000265631.9:c.2018G>C	ENSP00000265631.5:p.Gly673Ala
ENST00000416240.6:c.2021G>C	ENSP00000400101.2:p.Gly674Ala
ENST00000494085.1:n.521G>C
NM_001160210.1:c.2021G>C	NP_001153682.1:p.Gly674Ala
NM_014251.2:c.2018G>C	NP_055066.1:p.Gly673Ala
NR_027662.1:n.2093G>C
XM_006715831.2:c.2051G>C	XP_006715894.1:p.Gly684Ala
XM_011515728.1:c.1166G>C	XP_011514030.1:p.Gly389Ala
XM_006715831.4:c.2051G>C	XP_006715894.1:p.Gly684Ala
XM_017011663.1:c.2009G>C	XP_016867152.1:p.Gly670Ala
XM_017011664.2:c.1166G>C	XP_016867153.1:p.Gly389Ala
XM_017011665.1:c.1166G>C	XP_016867154.1:p.Gly389Ala
XR_001744525.2:n.2264G>C
XR_002956405.1:n.2822G>C
NM_014251.3:c.2018G>C MANE Select	NP_055066.1:p.Gly673Ala
NR_027662.2:n.2044G>C
NM_001160210.2:c.2021G>C	NP_001153682.1:p.Gly674Ala