Canonical Allele Identifier: CA163521938

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96296955T>C , CM000669.2:g.96296955T>C	GRCh38
NC_000007.13:g.95926267T>C , CM000669.1:g.95926267T>C	GRCh37
NC_000007.12:g.95764203T>C	NCBI36
NG_012247.1:g.30193A>G
NG_012247.2:g.30193A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.16-4A>G MANE Select	NP_055066.1:n.16-4A>G
ENST00000265631.10:c.16-4A>G MANE Select	ENSP00000265631.6:n.16-4A>G
NM_001160210.1:c.16-4A>G	NP_001153682.1:n.16-4A>G
NM_001160210.2:c.16-4A>G	NP_001153682.1:n.16-4A>G
NM_014251.2:c.16-4A>G	NP_055066.1:n.16-4A>G
NR_027662.1:n.207-4A>G
NR_027662.2:n.158-4A>G
ENST00000265631.9:c.16-4A>G	ENSP00000265631.5:n.16-4A>G
ENST00000416240.6:c.16-4A>G	ENSP00000400101.2:n.16-4A>G
ENST00000472162.2:c.16-4A>G	ENSP00000473505.1:n.16-4A>G
ENST00000487710.1:n.148-4A>G
XM_006715831.2:c.49-4A>G	XP_006715894.1:n.49-4A>G
XM_006715831.4:c.49-4A>G	XP_006715894.1:n.49-4A>G
XM_011515727.1:c.49-4A>G	XP_011514029.1:n.49-4A>G
XM_011515727.3:c.49-4A>G	XP_011514029.1:n.49-4A>G
XM_017011664.2:c.-743-4A>G	XP_016867153.1:n.-743-4A>G
XM_017011665.1:c.-627-4A>G	XP_016867154.1:n.-627-4A>G
XR_001744525.2:n.187-4A>G
XR_002956405.1:n.329-4A>G