Canonical Allele Identifier: CA456509872

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1791490761
• MyVariant Identifiers: chr7:g.95750584C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121272C>T , CM000669.2:g.96121272C>T	GRCh38
NC_000007.13:g.95750584C>T , CM000669.1:g.95750584C>T	GRCh37
NC_000007.12:g.95588520C>T	NCBI36
NG_012247.1:g.205876G>A
NG_012247.2:g.205876G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1947G>A MANE Select	ENSP00000265631.6:p.Gly649=
ENST00000265631.9:c.1947G>A	ENSP00000265631.5:p.Gly649=
ENST00000416240.6:c.1950G>A	ENSP00000400101.2:p.Gly650=
ENST00000494085.1:n.450G>A
NM_001160210.1:c.1950G>A	NP_001153682.1:p.Gly650=
NM_014251.2:c.1947G>A	NP_055066.1:p.Gly649=
NR_027662.1:n.2022G>A
XM_006715831.2:c.1980G>A	XP_006715894.1:p.Gly660=
XM_011515728.1:c.1095G>A	XP_011514030.1:p.Gly365=
XM_006715831.4:c.1980G>A	XP_006715894.1:p.Gly660=
XM_017011663.1:c.1938G>A	XP_016867152.1:p.Gly646=
XM_017011664.2:c.1095G>A	XP_016867153.1:p.Gly365=
XM_017011665.1:c.1095G>A	XP_016867154.1:p.Gly365=
XR_001744525.2:n.2193G>A
XR_002956405.1:n.2751G>A
NM_014251.3:c.1947G>A MANE Select	NP_055066.1:p.Gly649=
NR_027662.2:n.1973G>A
NM_001160210.2:c.1950G>A	NP_001153682.1:p.Gly650=