Canonical Allele Identifier: CA844193551

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1325868663
• gnomAD v3: 7-96189478-G-C
• gnomAD v4: 7-96189478-G-C
• MyVariant Identifiers: chr7:g.95818790G>C (hg19) ; chr7:g.96189478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189478G>C , CM000669.2:g.96189478G>C	GRCh38
NC_000007.13:g.95818790G>C , CM000669.1:g.95818790G>C	GRCh37
NC_000007.12:g.95656726G>C	NCBI36
NG_012247.1:g.137670C>G
NG_012247.2:g.137670C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-100C>G MANE Select	ENSP00000265631.6:n.849-100C>G
ENST00000265631.9:c.849-100C>G	ENSP00000265631.5:n.849-100C>G
ENST00000416240.6:c.849-100C>G	ENSP00000400101.2:n.849-100C>G
NM_001160210.1:c.849-100C>G	NP_001153682.1:n.849-100C>G
NM_014251.2:c.849-100C>G	NP_055066.1:n.849-100C>G
NR_027662.1:n.924-100C>G
XM_006715831.2:c.882-100C>G	XP_006715894.1:n.882-100C>G
XM_011515727.1:c.882-100C>G	XP_011514029.1:n.882-100C>G
XM_011515728.1:c.-4-100C>G	XP_011514030.1:n.-4-100C>G
XM_006715831.4:c.882-100C>G	XP_006715894.1:n.882-100C>G
XM_011515727.3:c.882-100C>G	XP_011514029.1:n.882-100C>G
XM_017011663.1:c.840-100C>G	XP_016867152.1:n.840-100C>G
XM_017011664.2:c.-4-100C>G	XP_016867153.1:n.-4-100C>G
XM_017011665.1:c.-4-100C>G	XP_016867154.1:n.-4-100C>G
XR_001744525.2:n.1020-100C>G
XR_002956405.1:n.1162-100C>G
NM_014251.3:c.849-100C>G MANE Select	NP_055066.1:n.849-100C>G
NR_027662.2:n.875-100C>G
NM_001160210.2:c.849-100C>G	NP_001153682.1:n.849-100C>G