Canonical Allele Identifier: CA368262319

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818671T>A (hg19) ; chr7:g.96189359T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189359T>A , CM000669.2:g.96189359T>A	GRCh38
NC_000007.13:g.95818671T>A , CM000669.1:g.95818671T>A	GRCh37
NC_000007.12:g.95656607T>A	NCBI36
NG_012247.1:g.137789A>T
NG_012247.2:g.137789A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.868A>T MANE Select	ENSP00000265631.6:p.Ile290Phe
ENST00000265631.9:c.868A>T	ENSP00000265631.5:p.Ile290Phe
ENST00000416240.6:c.868A>T	ENSP00000400101.2:p.Ile290Phe
ENST00000484495.5:n.21A>T
NM_001160210.1:c.868A>T	NP_001153682.1:p.Ile290Phe
NM_014251.2:c.868A>T	NP_055066.1:p.Ile290Phe
NR_027662.1:n.943A>T
XM_006715831.2:c.901A>T	XP_006715894.1:p.Ile301Phe
XM_011515727.1:c.901A>T	XP_011514029.1:p.Ile301Phe
XM_011515728.1:c.16A>T	XP_011514030.1:p.Ile6Phe
XM_006715831.4:c.901A>T	XP_006715894.1:p.Ile301Phe
XM_011515727.3:c.901A>T	XP_011514029.1:p.Ile301Phe
XM_017011663.1:c.859A>T	XP_016867152.1:p.Ile287Phe
XM_017011664.2:c.16A>T	XP_016867153.1:p.Ile6Phe
XM_017011665.1:c.16A>T	XP_016867154.1:p.Ile6Phe
XR_001744525.2:n.1039A>T
XR_002956405.1:n.1181A>T
NM_014251.3:c.868A>T MANE Select	NP_055066.1:p.Ile290Phe
NR_027662.2:n.894A>T
NM_001160210.2:c.868A>T	NP_001153682.1:p.Ile290Phe