Canonical Allele Identifier: CA4352888

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96131828C>T , CM000669.2:g.96131828C>T	GRCh38
NC_000007.13:g.95761140C>T , CM000669.1:g.95761140C>T	GRCh37
NC_000007.12:g.95599076C>T	NCBI36
NG_012247.1:g.195320G>A
NG_012247.2:g.195320G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.1506G>A MANE Select	NP_055066.1:p.Pro502=
ENST00000265631.10:c.1506G>A MANE Select	ENSP00000265631.6:p.Pro502=
NM_001160210.1:c.1509G>A	NP_001153682.1:p.Pro503=
NM_001160210.2:c.1509G>A	NP_001153682.1:p.Pro503=
NM_014251.2:c.1506G>A	NP_055066.1:p.Pro502=
NR_027662.1:n.1581G>A
NR_027662.2:n.1532G>A
ENST00000265631.9:c.1506G>A	ENSP00000265631.5:p.Pro502=
ENST00000416240.6:c.1509G>A	ENSP00000400101.2:p.Pro503=
XM_006715831.2:c.1539G>A	XP_006715894.1:p.Pro513=
XM_006715831.4:c.1539G>A	XP_006715894.1:p.Pro513=
XM_011515728.1:c.654G>A	XP_011514030.1:p.Pro218=
XM_017011663.1:c.1497G>A	XP_016867152.1:p.Pro499=
XM_017011664.2:c.654G>A	XP_016867153.1:p.Pro218=
XM_017011665.1:c.654G>A	XP_016867154.1:p.Pro218=
XR_001744525.2:n.1752G>A
XR_002956405.1:n.2310G>A