Canonical Allele Identifier: CA368257202

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750579T>G (hg19) ; chr7:g.96121267T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121267T>G , CM000669.2:g.96121267T>G	GRCh38
NC_000007.13:g.95750579T>G , CM000669.1:g.95750579T>G	GRCh37
NC_000007.12:g.95588515T>G	NCBI36
NG_012247.1:g.205881A>C
NG_012247.2:g.205881A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1952A>C MANE Select	ENSP00000265631.6:p.Glu651Ala
ENST00000265631.9:c.1952A>C	ENSP00000265631.5:p.Glu651Ala
ENST00000416240.6:c.1955A>C	ENSP00000400101.2:p.Glu652Ala
ENST00000494085.1:n.455A>C
NM_001160210.1:c.1955A>C	NP_001153682.1:p.Glu652Ala
NM_014251.2:c.1952A>C	NP_055066.1:p.Glu651Ala
NR_027662.1:n.2027A>C
XM_006715831.2:c.1985A>C	XP_006715894.1:p.Glu662Ala
XM_011515728.1:c.1100A>C	XP_011514030.1:p.Glu367Ala
XM_006715831.4:c.1985A>C	XP_006715894.1:p.Glu662Ala
XM_017011663.1:c.1943A>C	XP_016867152.1:p.Glu648Ala
XM_017011664.2:c.1100A>C	XP_016867153.1:p.Glu367Ala
XM_017011665.1:c.1100A>C	XP_016867154.1:p.Glu367Ala
XR_001744525.2:n.2198A>C
XR_002956405.1:n.2756A>C
NM_014251.3:c.1952A>C MANE Select	NP_055066.1:p.Glu651Ala
NR_027662.2:n.1978A>C
NM_001160210.2:c.1955A>C	NP_001153682.1:p.Glu652Ala