Canonical Allele Identifier: CA4353129

Gene: SLC25A13

Linked Data

• dbSNP Id: rs751513644
• ExAC: 7:95818739 A / G
• gnomAD v2: 7-95818739-A-G
• gnomAD v3: 7-96189427-A-G
• gnomAD v4: 7-96189427-A-G
• MyVariant Identifiers: chr7:g.95818739A>G (hg19) ; chr7:g.96189427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189427A>G , CM000669.2:g.96189427A>G	GRCh38
NC_000007.13:g.95818739A>G , CM000669.1:g.95818739A>G	GRCh37
NC_000007.12:g.95656675A>G	NCBI36
NG_012247.1:g.137721T>C
NG_012247.2:g.137721T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-49T>C MANE Select	ENSP00000265631.6:n.849-49T>C
ENST00000265631.9:c.849-49T>C	ENSP00000265631.5:n.849-49T>C
ENST00000416240.6:c.849-49T>C	ENSP00000400101.2:n.849-49T>C
NM_001160210.1:c.849-49T>C	NP_001153682.1:n.849-49T>C
NM_014251.2:c.849-49T>C	NP_055066.1:n.849-49T>C
NR_027662.1:n.924-49T>C
XM_006715831.2:c.882-49T>C	XP_006715894.1:n.882-49T>C
XM_011515727.1:c.882-49T>C	XP_011514029.1:n.882-49T>C
XM_011515728.1:c.-4-49T>C	XP_011514030.1:n.-4-49T>C
XM_006715831.4:c.882-49T>C	XP_006715894.1:n.882-49T>C
XM_011515727.3:c.882-49T>C	XP_011514029.1:n.882-49T>C
XM_017011663.1:c.840-49T>C	XP_016867152.1:n.840-49T>C
XM_017011664.2:c.-4-49T>C	XP_016867153.1:n.-4-49T>C
XM_017011665.1:c.-4-49T>C	XP_016867154.1:n.-4-49T>C
XR_001744525.2:n.1020-49T>C
XR_002956405.1:n.1162-49T>C
NM_014251.3:c.849-49T>C MANE Select	NP_055066.1:n.849-49T>C
NR_027662.2:n.875-49T>C
NM_001160210.2:c.849-49T>C	NP_001153682.1:n.849-49T>C