Canonical Allele Identifier: CA368258125

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751199T>A (hg19) ; chr7:g.96121887T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121887T>A , CM000669.2:g.96121887T>A	GRCh38
NC_000007.13:g.95751199T>A , CM000669.1:g.95751199T>A	GRCh37
NC_000007.12:g.95589135T>A	NCBI36
NG_012247.1:g.205261A>T
NG_012247.2:g.205261A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1702A>T MANE Select	ENSP00000265631.6:p.Lys568Ter
ENST00000265631.9:c.1702A>T	ENSP00000265631.5:p.Lys568Ter
ENST00000416240.6:c.1705A>T	ENSP00000400101.2:p.Lys569Ter
ENST00000494085.1:n.112A>T
NM_001160210.1:c.1705A>T	NP_001153682.1:p.Lys569Ter
NM_014251.2:c.1702A>T	NP_055066.1:p.Lys568Ter
NR_027662.1:n.1777A>T
XM_006715831.2:c.1735A>T	XP_006715894.1:p.Lys579Ter
XM_011515728.1:c.850A>T	XP_011514030.1:p.Lys284Ter
XM_006715831.4:c.1735A>T	XP_006715894.1:p.Lys579Ter
XM_017011663.1:c.1693A>T	XP_016867152.1:p.Lys565Ter
XM_017011664.2:c.850A>T	XP_016867153.1:p.Lys284Ter
XM_017011665.1:c.850A>T	XP_016867154.1:p.Lys284Ter
XR_001744525.2:n.1948A>T
XR_002956405.1:n.2506A>T
NM_014251.3:c.1702A>T MANE Select	NP_055066.1:p.Lys568Ter
NR_027662.2:n.1728A>T
NM_001160210.2:c.1705A>T	NP_001153682.1:p.Lys569Ter