Canonical Allele Identifier: CA576707821

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1176265608
• gnomAD v2: 7-95751351-T-C
• gnomAD v4: 7-96122039-T-C
• MyVariant Identifiers: chr7:g.95751351T>C (hg19) ; chr7:g.96122039T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122039T>C , CM000669.2:g.96122039T>C	GRCh38
NC_000007.13:g.95751351T>C , CM000669.1:g.95751351T>C	GRCh37
NC_000007.12:g.95589287T>C	NCBI36
NG_012247.1:g.205109A>G
NG_012247.2:g.205109A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-42A>G MANE Select	ENSP00000265631.6:n.1592-42A>G
ENST00000265631.9:c.1592-42A>G	ENSP00000265631.5:n.1592-42A>G
ENST00000416240.6:c.1595-42A>G	ENSP00000400101.2:n.1595-42A>G
NM_001160210.1:c.1595-42A>G	NP_001153682.1:n.1595-42A>G
NM_014251.2:c.1592-42A>G	NP_055066.1:n.1592-42A>G
NR_027662.1:n.1667-42A>G
XM_006715831.2:c.1625-42A>G	XP_006715894.1:n.1625-42A>G
XM_011515728.1:c.740-42A>G	XP_011514030.1:n.740-42A>G
XM_006715831.4:c.1625-42A>G	XP_006715894.1:n.1625-42A>G
XM_017011663.1:c.1583-42A>G	XP_016867152.1:n.1583-42A>G
XM_017011664.2:c.740-42A>G	XP_016867153.1:n.740-42A>G
XM_017011665.1:c.740-42A>G	XP_016867154.1:n.740-42A>G
XR_001744525.2:n.1838-42A>G
XR_002956405.1:n.2396-42A>G
NM_014251.3:c.1592-42A>G MANE Select	NP_055066.1:n.1592-42A>G
NR_027662.2:n.1618-42A>G
NM_001160210.2:c.1595-42A>G	NP_001153682.1:n.1595-42A>G