Canonical Allele Identifier: CA456510027

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750683G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121371G>C , CM000669.2:g.96121371G>C	GRCh38
NC_000007.13:g.95750683G>C , CM000669.1:g.95750683G>C	GRCh37
NC_000007.12:g.95588619G>C	NCBI36
NG_012247.1:g.205777C>G
NG_012247.2:g.205777C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1848C>G MANE Select	ENSP00000265631.6:p.Pro616=
ENST00000265631.9:c.1848C>G	ENSP00000265631.5:p.Pro616=
ENST00000416240.6:c.1851C>G	ENSP00000400101.2:p.Pro617=
ENST00000494085.1:n.351C>G
NM_001160210.1:c.1851C>G	NP_001153682.1:p.Pro617=
NM_014251.2:c.1848C>G	NP_055066.1:p.Pro616=
NR_027662.1:n.1923C>G
XM_006715831.2:c.1881C>G	XP_006715894.1:p.Pro627=
XM_011515728.1:c.996C>G	XP_011514030.1:p.Pro332=
XM_006715831.4:c.1881C>G	XP_006715894.1:p.Pro627=
XM_017011663.1:c.1839C>G	XP_016867152.1:p.Pro613=
XM_017011664.2:c.996C>G	XP_016867153.1:p.Pro332=
XM_017011665.1:c.996C>G	XP_016867154.1:p.Pro332=
XR_001744525.2:n.2094C>G
XR_002956405.1:n.2652C>G
NM_014251.3:c.1848C>G MANE Select	NP_055066.1:p.Pro616=
NR_027662.2:n.1874C>G
NM_001160210.2:c.1851C>G	NP_001153682.1:p.Pro617=