Canonical Allele Identifier: CA4353385

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96277315A>G , CM000669.2:g.96277315A>G	GRCh38
NC_000007.13:g.95906627A>G , CM000669.1:g.95906627A>G	GRCh37
NC_000007.12:g.95744563A>G	NCBI36
NG_012247.1:g.49833T>C
NG_012247.2:g.49833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.93T>C MANE Select	ENSP00000265631.6:p.Gly31=
ENST00000265631.9:c.93T>C	ENSP00000265631.5:p.Gly31=
ENST00000416240.6:c.93T>C	ENSP00000400101.2:p.Gly31=
ENST00000472162.2:c.93T>C	ENSP00000473505.1:p.Gly31=
NM_001160210.1:c.93T>C	NP_001153682.1:p.Gly31=
NM_014251.2:c.93T>C	NP_055066.1:p.Gly31=
NR_027662.1:n.284T>C
XM_006715831.2:c.126T>C	XP_006715894.1:p.Gly42=
XM_011515727.1:c.126T>C	XP_011514029.1:p.Gly42=
XM_006715831.4:c.126T>C	XP_006715894.1:p.Gly42=
XM_011515727.3:c.126T>C	XP_011514029.1:p.Gly42=
XM_017011663.1:c.84T>C	XP_016867152.1:p.Gly28=
XM_017011664.2:c.-666T>C	XP_016867153.1:n.-666T>C
XM_017011665.1:c.-550T>C	XP_016867154.1:n.-550T>C
XR_001744525.2:n.264T>C
XR_002956405.1:n.406T>C
NM_014251.3:c.93T>C MANE Select	NP_055066.1:p.Gly31=
NR_027662.2:n.235T>C
NM_001160210.2:c.93T>C	NP_001153682.1:p.Gly31=