Canonical Allele Identifier: CA2697557415

Gene: SLC25A13

Linked Data

• ClinVar Variation Id: 2699545
• ClinVar RCV Id: RCV003582223

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122006G>C , CM000669.2:g.96122006G>C	GRCh38
NC_000007.13:g.95751318G>C , CM000669.1:g.95751318G>C	GRCh37
NC_000007.12:g.95589254G>C	NCBI36
NG_012247.1:g.205142C>G
NG_012247.2:g.205142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-9C>G MANE Select	ENSP00000265631.6:n.1592-9C>G
ENST00000265631.9:c.1592-9C>G	ENSP00000265631.5:n.1592-9C>G
ENST00000416240.6:c.1595-9C>G	ENSP00000400101.2:n.1595-9C>G
NM_001160210.1:c.1595-9C>G	NP_001153682.1:n.1595-9C>G
NM_014251.2:c.1592-9C>G	NP_055066.1:n.1592-9C>G
NR_027662.1:n.1667-9C>G
XM_006715831.2:c.1625-9C>G	XP_006715894.1:n.1625-9C>G
XM_011515728.1:c.740-9C>G	XP_011514030.1:n.740-9C>G
XM_006715831.4:c.1625-9C>G	XP_006715894.1:n.1625-9C>G
XM_017011663.1:c.1583-9C>G	XP_016867152.1:n.1583-9C>G
XM_017011664.2:c.740-9C>G	XP_016867153.1:n.740-9C>G
XM_017011665.1:c.740-9C>G	XP_016867154.1:n.740-9C>G
XR_001744525.2:n.1838-9C>G
XR_002956405.1:n.2396-9C>G
NM_014251.3:c.1592-9C>G MANE Select	NP_055066.1:n.1592-9C>G
NR_027662.2:n.1618-9C>G
NM_001160210.2:c.1595-9C>G	NP_001153682.1:n.1595-9C>G