Canonical Allele Identifier: CA576707787

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1229840236
• gnomAD v2: 7-95818721-A-AAC
• MyVariant Identifiers: chr7:g.95818721_95818722insAC (hg19) ; chr7:g.96189409_96189410insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189409_96189410insAC , CM000669.2:g.96189409_96189410insAC	GRCh38
NC_000007.13:g.95818721_95818722insAC , CM000669.1:g.95818721_95818722insAC	GRCh37
NC_000007.12:g.95656657_95656658insAC	NCBI36
NG_012247.1:g.137738_137739insGT
NG_012247.2:g.137738_137739insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-32_849-31insGT MANE Select	ENSP00000265631.6:n.849-32_849-31insGT
ENST00000265631.9:c.849-32_849-31insGT	ENSP00000265631.5:n.849-32_849-31insGT
ENST00000416240.6:c.849-32_849-31insGT	ENSP00000400101.2:n.849-32_849-31insGT
NM_001160210.1:c.849-32_849-31insGT	NP_001153682.1:n.849-32_849-31insGT
NM_014251.2:c.849-32_849-31insGT	NP_055066.1:n.849-32_849-31insGT
NR_027662.1:n.924-32_924-31insGT
XM_006715831.2:c.882-32_882-31insGT	XP_006715894.1:n.882-32_882-31insGT
XM_011515727.1:c.882-32_882-31insGT	XP_011514029.1:n.882-32_882-31insGT
XM_011515728.1:c.-4-32_-4-31insGT	XP_011514030.1:n.-4-32_-4-31insGT
XM_006715831.4:c.882-32_882-31insGT	XP_006715894.1:n.882-32_882-31insGT
XM_011515727.3:c.882-32_882-31insGT	XP_011514029.1:n.882-32_882-31insGT
XM_017011663.1:c.840-32_840-31insGT	XP_016867152.1:n.840-32_840-31insGT
XM_017011664.2:c.-4-32_-4-31insGT	XP_016867153.1:n.-4-32_-4-31insGT
XM_017011665.1:c.-4-32_-4-31insGT	XP_016867154.1:n.-4-32_-4-31insGT
XR_001744525.2:n.1020-32_1020-31insGT
XR_002956405.1:n.1162-32_1162-31insGT
NM_014251.3:c.849-32_849-31insGT MANE Select	NP_055066.1:n.849-32_849-31insGT
NR_027662.2:n.875-32_875-31insGT
NM_001160210.2:c.849-32_849-31insGT	NP_001153682.1:n.849-32_849-31insGT