Canonical Allele Identifier: CA10586124

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121261T>C , CM000669.2:g.96121261T>C	GRCh38
NC_000007.13:g.95750573T>C , CM000669.1:g.95750573T>C	GRCh37
NC_000007.12:g.95588509T>C	NCBI36
NG_012247.1:g.205887A>G
NG_012247.2:g.205887A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.1958A>G MANE Select	NP_055066.1:p.Lys653Arg
ENST00000265631.10:c.1958A>G MANE Select	ENSP00000265631.6:p.Lys653Arg
NM_001160210.1:c.1961A>G	NP_001153682.1:p.Lys654Arg
NM_001160210.2:c.1961A>G	NP_001153682.1:p.Lys654Arg
NM_014251.2:c.1958A>G	NP_055066.1:p.Lys653Arg
NR_027662.1:n.2033A>G
NR_027662.2:n.1984A>G
ENST00000265631.9:c.1958A>G	ENSP00000265631.5:p.Lys653Arg
ENST00000416240.6:c.1961A>G	ENSP00000400101.2:p.Lys654Arg
ENST00000494085.1:n.461A>G
XM_006715831.2:c.1991A>G	XP_006715894.1:p.Lys664Arg
XM_006715831.4:c.1991A>G	XP_006715894.1:p.Lys664Arg
XM_011515728.1:c.1106A>G	XP_011514030.1:p.Lys369Arg
XM_017011663.1:c.1949A>G	XP_016867152.1:p.Lys650Arg
XM_017011664.2:c.1106A>G	XP_016867153.1:p.Lys369Arg
XM_017011665.1:c.1106A>G	XP_016867154.1:p.Lys369Arg
XR_001744525.2:n.2204A>G
XR_002956405.1:n.2762A>G