Canonical Allele Identifier: CA368263281

Gene: SLC25A13

Linked Data

• dbSNP Id: rs2116662596
• MyVariant Identifiers: chr7:g.95822359C>G (hg19) ; chr7:g.96193047C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193047C>G , CM000669.2:g.96193047C>G	GRCh38
NC_000007.13:g.95822359C>G , CM000669.1:g.95822359C>G	GRCh37
NC_000007.12:g.95660295C>G	NCBI36
NG_012247.1:g.134101G>C
NG_012247.2:g.134101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.605G>C MANE Select	ENSP00000265631.6:p.Cys202Ser
ENST00000265631.9:c.605G>C	ENSP00000265631.5:p.Cys202Ser
ENST00000416240.6:c.605G>C	ENSP00000400101.2:p.Cys202Ser
NM_001160210.1:c.605G>C	NP_001153682.1:p.Cys202Ser
NM_014251.2:c.605G>C	NP_055066.1:p.Cys202Ser
NR_027662.1:n.680G>C
XM_006715831.2:c.638G>C	XP_006715894.1:p.Cys213Ser
XM_011515727.1:c.638G>C	XP_011514029.1:p.Cys213Ser
XM_006715831.4:c.638G>C	XP_006715894.1:p.Cys213Ser
XM_011515727.3:c.638G>C	XP_011514029.1:p.Cys213Ser
XM_017011663.1:c.596G>C	XP_016867152.1:p.Cys199Ser
XM_017011664.2:c.-154G>C	XP_016867153.1:n.-154G>C
XM_017011665.1:c.-154G>C	XP_016867154.1:n.-154G>C
XR_001744525.2:n.776G>C
XR_002956405.1:n.918G>C
NM_014251.3:c.605G>C MANE Select	NP_055066.1:p.Cys202Ser
NR_027662.2:n.631G>C
NM_001160210.2:c.605G>C	NP_001153682.1:p.Cys202Ser