Canonical Allele Identifier: CA456510829

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818611T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189299T>G , CM000669.2:g.96189299T>G	GRCh38
NC_000007.13:g.95818611T>G , CM000669.1:g.95818611T>G	GRCh37
NC_000007.12:g.95656547T>G	NCBI36
NG_012247.1:g.137849A>C
NG_012247.2:g.137849A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.928A>C MANE Select	ENSP00000265631.6:p.Arg310=
ENST00000265631.9:c.928A>C	ENSP00000265631.5:p.Arg310=
ENST00000416240.6:c.928A>C	ENSP00000400101.2:p.Arg310=
ENST00000484495.5:n.81A>C
NM_001160210.1:c.928A>C	NP_001153682.1:p.Arg310=
NM_014251.2:c.928A>C	NP_055066.1:p.Arg310=
NR_027662.1:n.1003A>C
XM_006715831.2:c.961A>C	XP_006715894.1:p.Arg321=
XM_011515727.1:c.961A>C	XP_011514029.1:p.Arg321=
XM_011515728.1:c.76A>C	XP_011514030.1:p.Arg26=
XM_006715831.4:c.961A>C	XP_006715894.1:p.Arg321=
XM_011515727.3:c.961A>C	XP_011514029.1:p.Arg321=
XM_017011663.1:c.919A>C	XP_016867152.1:p.Arg307=
XM_017011664.2:c.76A>C	XP_016867153.1:p.Arg26=
XM_017011665.1:c.76A>C	XP_016867154.1:p.Arg26=
XR_001744525.2:n.1099A>C
XR_002956405.1:n.1241A>C
NM_014251.3:c.928A>C MANE Select	NP_055066.1:p.Arg310=
NR_027662.2:n.954A>C
NM_001160210.2:c.928A>C	NP_001153682.1:p.Arg310=