Canonical Allele Identifier: CA4352679

Gene: SLC25A13

Linked Data

• ClinVar Variation Id: 361001
• ClinVar RCV Id: RCV000275604 ; RCV000385869
• dbSNP Id: rs373153995
• ExAC: 7:95749774 C / T
• gnomAD v2: 7-95749774-C-T
• gnomAD v3: 7-96120462-C-T
• gnomAD v4: 7-96120462-C-T
• MyVariant Identifiers: chr7:g.95749774C>T (hg19) ; chr7:g.96120462C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96120462C>T , CM000669.2:g.96120462C>T	GRCh38
NC_000007.13:g.95749774C>T , CM000669.1:g.95749774C>T	GRCh37
NC_000007.12:g.95587710C>T	NCBI36
NG_012247.1:g.206686G>A
NG_012247.2:g.206686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.*729G>A MANE Select	ENSP00000265631.6:n.*729G>A
ENST00000265631.9:c.*729G>A	ENSP00000265631.5:n.*729G>A
ENST00000416240.6:c.*729G>A	ENSP00000400101.2:n.*729G>A
NM_001160210.1:c.*729G>A	NP_001153682.1:n.*729G>A
NM_014251.2:c.*729G>A	NP_055066.1:n.*729G>A
NR_027662.1:n.2832G>A
XM_006715831.2:c.*729G>A	XP_006715894.1:n.*729G>A
XM_011515728.1:c.*729G>A	XP_011514030.1:n.*729G>A
XM_006715831.4:c.*729G>A	XP_006715894.1:n.*729G>A
XM_017011663.1:c.*729G>A	XP_016867152.1:n.*729G>A
XM_017011664.2:c.*729G>A	XP_016867153.1:n.*729G>A
XM_017011665.1:c.*729G>A	XP_016867154.1:n.*729G>A
XR_001744525.2:n.3003G>A
XR_002956405.1:n.3561G>A
NM_014251.3:c.*729G>A MANE Select	NP_055066.1:n.*729G>A
NR_027662.2:n.2783G>A
NM_001160210.2:c.*729G>A	NP_001153682.1:n.*729G>A