Canonical Allele Identifier: CA456509812

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750527T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121215T>G , CM000669.2:g.96121215T>G	GRCh38
NC_000007.13:g.95750527T>G , CM000669.1:g.95750527T>G	GRCh37
NC_000007.12:g.95588463T>G	NCBI36
NG_012247.1:g.205933A>C
NG_012247.2:g.205933A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.2004A>C MANE Select	ENSP00000265631.6:p.Ser668=
ENST00000265631.9:c.2004A>C	ENSP00000265631.5:p.Ser668=
ENST00000416240.6:c.2007A>C	ENSP00000400101.2:p.Ser669=
ENST00000494085.1:n.507A>C
NM_001160210.1:c.2007A>C	NP_001153682.1:p.Ser669=
NM_014251.2:c.2004A>C	NP_055066.1:p.Ser668=
NR_027662.1:n.2079A>C
XM_006715831.2:c.2037A>C	XP_006715894.1:p.Ser679=
XM_011515728.1:c.1152A>C	XP_011514030.1:p.Ser384=
XM_006715831.4:c.2037A>C	XP_006715894.1:p.Ser679=
XM_017011663.1:c.1995A>C	XP_016867152.1:p.Ser665=
XM_017011664.2:c.1152A>C	XP_016867153.1:p.Ser384=
XM_017011665.1:c.1152A>C	XP_016867154.1:p.Ser384=
XR_001744525.2:n.2250A>C
XR_002956405.1:n.2808A>C
NM_014251.3:c.2004A>C MANE Select	NP_055066.1:p.Ser668=
NR_027662.2:n.2030A>C
NM_001160210.2:c.2007A>C	NP_001153682.1:p.Ser669=