Canonical Allele Identifier: CA4352946

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96146634C>T , CM000669.2:g.96146634C>T	GRCh38
NC_000007.13:g.95775946C>T , CM000669.1:g.95775946C>T	GRCh37
NC_000007.12:g.95613882C>T	NCBI36
NG_012247.1:g.180514G>A
NG_012247.2:g.180514G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.1374G>A MANE Select	NP_055066.1:p.Val458=
ENST00000265631.10:c.1374G>A MANE Select	ENSP00000265631.6:p.Val458=
NM_001160210.1:c.1377G>A	NP_001153682.1:p.Val459=
NM_001160210.2:c.1377G>A	NP_001153682.1:p.Val459=
NM_014251.2:c.1374G>A	NP_055066.1:p.Val458=
NR_027662.1:n.1449G>A
NR_027662.2:n.1400G>A
ENST00000265631.9:c.1374G>A	ENSP00000265631.5:p.Val458=
ENST00000416240.6:c.1377G>A	ENSP00000400101.2:p.Val459=
ENST00000490072.5:n.498G>A
XM_006715831.2:c.1407G>A	XP_006715894.1:p.Val469=
XM_006715831.4:c.1407G>A	XP_006715894.1:p.Val469=
XM_011515727.1:c.*111G>A	XP_011514029.1:n.*111G>A
XM_011515727.3:c.*111G>A	XP_011514029.1:n.*111G>A
XM_011515728.1:c.522G>A	XP_011514030.1:p.Val174=
XM_017011663.1:c.1365G>A	XP_016867152.1:p.Val455=
XM_017011664.2:c.522G>A	XP_016867153.1:p.Val174=
XM_017011665.1:c.522G>A	XP_016867154.1:p.Val174=
XR_001744525.2:n.1620G>A
XR_002956405.1:n.2178G>A