Canonical Allele Identifier: CA456632281

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751194T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121882T>A , CM000669.2:g.96121882T>A	GRCh38
NC_000007.13:g.95751194T>A , CM000669.1:g.95751194T>A	GRCh37
NC_000007.12:g.95589130T>A	NCBI36
NG_012247.1:g.205266A>T
NG_012247.2:g.205266A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1707A>T MANE Select	ENSP00000265631.6:p.Ile569=
ENST00000265631.9:c.1707A>T	ENSP00000265631.5:p.Ile569=
ENST00000416240.6:c.1710A>T	ENSP00000400101.2:p.Ile570=
ENST00000494085.1:n.117A>T
NM_001160210.1:c.1710A>T	NP_001153682.1:p.Ile570=
NM_014251.2:c.1707A>T	NP_055066.1:p.Ile569=
NR_027662.1:n.1782A>T
XM_006715831.2:c.1740A>T	XP_006715894.1:p.Ile580=
XM_011515728.1:c.855A>T	XP_011514030.1:p.Ile285=
XM_006715831.4:c.1740A>T	XP_006715894.1:p.Ile580=
XM_017011663.1:c.1698A>T	XP_016867152.1:p.Ile566=
XM_017011664.2:c.855A>T	XP_016867153.1:p.Ile285=
XM_017011665.1:c.855A>T	XP_016867154.1:p.Ile285=
XR_001744525.2:n.1953A>T
XR_002956405.1:n.2511A>T
NM_014251.3:c.1707A>T MANE Select	NP_055066.1:p.Ile569=
NR_027662.2:n.1733A>T
NM_001160210.2:c.1710A>T	NP_001153682.1:p.Ile570=