Canonical Allele Identifier: CA576707877

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1407125347
• gnomAD v2: 7-95818863-C-CA
• gnomAD v3: 7-96189551-C-CA
• gnomAD v4: 7-96189551-C-CA
• MyVariant Identifiers: chr7:g.95818863_95818864insA (hg19) ; chr7:g.96189551_96189552insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189551_96189552insA , CM000669.2:g.96189551_96189552insA	GRCh38
NC_000007.13:g.95818863_95818864insA , CM000669.1:g.95818863_95818864insA	GRCh37
NC_000007.12:g.95656799_95656800insA	NCBI36
NG_012247.1:g.137596_137597insT
NG_012247.2:g.137596_137597insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+29_848+30insT MANE Select	ENSP00000265631.6:n.848+29_848+30insT
ENST00000265631.9:c.848+29_848+30insT	ENSP00000265631.5:n.848+29_848+30insT
ENST00000416240.6:c.848+29_848+30insT	ENSP00000400101.2:n.848+29_848+30insT
NM_001160210.1:c.848+29_848+30insT	NP_001153682.1:n.848+29_848+30insT
NM_014251.2:c.848+29_848+30insT	NP_055066.1:n.848+29_848+30insT
NR_027662.1:n.923+29_923+30insT
XM_006715831.2:c.881+29_881+30insT	XP_006715894.1:n.881+29_881+30insT
XM_011515727.1:c.881+29_881+30insT	XP_011514029.1:n.881+29_881+30insT
XM_011515728.1:c.-4-174_-4-173insT	XP_011514030.1:n.-4-174_-4-173insT
XM_006715831.4:c.881+29_881+30insT	XP_006715894.1:n.881+29_881+30insT
XM_011515727.3:c.881+29_881+30insT	XP_011514029.1:n.881+29_881+30insT
XM_017011663.1:c.839+29_839+30insT	XP_016867152.1:n.839+29_839+30insT
XM_017011664.2:c.-4-174_-4-173insT	XP_016867153.1:n.-4-174_-4-173insT
XM_017011665.1:c.-4-174_-4-173insT	XP_016867154.1:n.-4-174_-4-173insT
XR_001744525.2:n.1019+29_1019+30insT
XR_002956405.1:n.1161+29_1161+30insT
NM_014251.3:c.848+29_848+30insT MANE Select	NP_055066.1:n.848+29_848+30insT
NR_027662.2:n.874+29_874+30insT
NM_001160210.2:c.848+29_848+30insT	NP_001153682.1:n.848+29_848+30insT