Canonical Allele Identifier: CA456509885

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750593T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121281T>A , CM000669.2:g.96121281T>A	GRCh38
NC_000007.13:g.95750593T>A , CM000669.1:g.95750593T>A	GRCh37
NC_000007.12:g.95588529T>A	NCBI36
NG_012247.1:g.205867A>T
NG_012247.2:g.205867A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1938A>T MANE Select	ENSP00000265631.6:p.Thr646=
ENST00000265631.9:c.1938A>T	ENSP00000265631.5:p.Thr646=
ENST00000416240.6:c.1941A>T	ENSP00000400101.2:p.Thr647=
ENST00000494085.1:n.441A>T
NM_001160210.1:c.1941A>T	NP_001153682.1:p.Thr647=
NM_014251.2:c.1938A>T	NP_055066.1:p.Thr646=
NR_027662.1:n.2013A>T
XM_006715831.2:c.1971A>T	XP_006715894.1:p.Thr657=
XM_011515728.1:c.1086A>T	XP_011514030.1:p.Thr362=
XM_006715831.4:c.1971A>T	XP_006715894.1:p.Thr657=
XM_017011663.1:c.1929A>T	XP_016867152.1:p.Thr643=
XM_017011664.2:c.1086A>T	XP_016867153.1:p.Thr362=
XM_017011665.1:c.1086A>T	XP_016867154.1:p.Thr362=
XR_001744525.2:n.2184A>T
XR_002956405.1:n.2742A>T
NM_014251.3:c.1938A>T MANE Select	NP_055066.1:p.Thr646=
NR_027662.2:n.1964A>T
NM_001160210.2:c.1941A>T	NP_001153682.1:p.Thr647=