Canonical Allele Identifier: CA368262242

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818655G>C (hg19) ; chr7:g.96189343G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189343G>C , CM000669.2:g.96189343G>C	GRCh38
NC_000007.13:g.95818655G>C , CM000669.1:g.95818655G>C	GRCh37
NC_000007.12:g.95656591G>C	NCBI36
NG_012247.1:g.137805C>G
NG_012247.2:g.137805C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.884C>G MANE Select	ENSP00000265631.6:p.Pro295Arg
ENST00000265631.9:c.884C>G	ENSP00000265631.5:p.Pro295Arg
ENST00000416240.6:c.884C>G	ENSP00000400101.2:p.Pro295Arg
ENST00000484495.5:n.37C>G
NM_001160210.1:c.884C>G	NP_001153682.1:p.Pro295Arg
NM_014251.2:c.884C>G	NP_055066.1:p.Pro295Arg
NR_027662.1:n.959C>G
XM_006715831.2:c.917C>G	XP_006715894.1:p.Pro306Arg
XM_011515727.1:c.917C>G	XP_011514029.1:p.Pro306Arg
XM_011515728.1:c.32C>G	XP_011514030.1:p.Pro11Arg
XM_006715831.4:c.917C>G	XP_006715894.1:p.Pro306Arg
XM_011515727.3:c.917C>G	XP_011514029.1:p.Pro306Arg
XM_017011663.1:c.875C>G	XP_016867152.1:p.Pro292Arg
XM_017011664.2:c.32C>G	XP_016867153.1:p.Pro11Arg
XM_017011665.1:c.32C>G	XP_016867154.1:p.Pro11Arg
XR_001744525.2:n.1055C>G
XR_002956405.1:n.1197C>G
NM_014251.3:c.884C>G MANE Select	NP_055066.1:p.Pro295Arg
NR_027662.2:n.910C>G
NM_001160210.2:c.884C>G	NP_001153682.1:p.Pro295Arg