Canonical Allele Identifier: CA456509904

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750602T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121290T>C , CM000669.2:g.96121290T>C	GRCh38
NC_000007.13:g.95750602T>C , CM000669.1:g.95750602T>C	GRCh37
NC_000007.12:g.95588538T>C	NCBI36
NG_012247.1:g.205858A>G
NG_012247.2:g.205858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1929A>G MANE Select	ENSP00000265631.6:p.Ala643=
ENST00000265631.9:c.1929A>G	ENSP00000265631.5:p.Ala643=
ENST00000416240.6:c.1932A>G	ENSP00000400101.2:p.Ala644=
ENST00000494085.1:n.432A>G
NM_001160210.1:c.1932A>G	NP_001153682.1:p.Ala644=
NM_014251.2:c.1929A>G	NP_055066.1:p.Ala643=
NR_027662.1:n.2004A>G
XM_006715831.2:c.1962A>G	XP_006715894.1:p.Ala654=
XM_011515728.1:c.1077A>G	XP_011514030.1:p.Ala359=
XM_006715831.4:c.1962A>G	XP_006715894.1:p.Ala654=
XM_017011663.1:c.1920A>G	XP_016867152.1:p.Ala640=
XM_017011664.2:c.1077A>G	XP_016867153.1:p.Ala359=
XM_017011665.1:c.1077A>G	XP_016867154.1:p.Ala359=
XR_001744525.2:n.2175A>G
XR_002956405.1:n.2733A>G
NM_014251.3:c.1929A>G MANE Select	NP_055066.1:p.Ala643=
NR_027662.2:n.1955A>G
NM_001160210.2:c.1932A>G	NP_001153682.1:p.Ala644=