Canonical Allele Identifier: CA576707788

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1281991696
• gnomAD v2: 7-95818722-T-TCTAG
• MyVariant Identifiers: chr7:g.95818722_95818723insCTAG (hg19) ; chr7:g.96189410_96189411insCTAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189410_96189411insCTAG , CM000669.2:g.96189410_96189411insCTAG	GRCh38
NC_000007.13:g.95818722_95818723insCTAG , CM000669.1:g.95818722_95818723insCTAG	GRCh37
NC_000007.12:g.95656658_95656659insCTAG	NCBI36
NG_012247.1:g.137737_137738insCTAG
NG_012247.2:g.137737_137738insCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-33_849-32insCTAG MANE Select	ENSP00000265631.6:n.849-33_849-32insCTAG
ENST00000265631.9:c.849-33_849-32insCTAG	ENSP00000265631.5:n.849-33_849-32insCTAG
ENST00000416240.6:c.849-33_849-32insCTAG	ENSP00000400101.2:n.849-33_849-32insCTAG
NM_001160210.1:c.849-33_849-32insCTAG	NP_001153682.1:n.849-33_849-32insCTAG
NM_014251.2:c.849-33_849-32insCTAG	NP_055066.1:n.849-33_849-32insCTAG
NR_027662.1:n.924-33_924-32insCTAG
XM_006715831.2:c.882-33_882-32insCTAG	XP_006715894.1:n.882-33_882-32insCTAG
XM_011515727.1:c.882-33_882-32insCTAG	XP_011514029.1:n.882-33_882-32insCTAG
XM_011515728.1:c.-4-33_-4-32insCTAG	XP_011514030.1:n.-4-33_-4-32insCTAG
XM_006715831.4:c.882-33_882-32insCTAG	XP_006715894.1:n.882-33_882-32insCTAG
XM_011515727.3:c.882-33_882-32insCTAG	XP_011514029.1:n.882-33_882-32insCTAG
XM_017011663.1:c.840-33_840-32insCTAG	XP_016867152.1:n.840-33_840-32insCTAG
XM_017011664.2:c.-4-33_-4-32insCTAG	XP_016867153.1:n.-4-33_-4-32insCTAG
XM_017011665.1:c.-4-33_-4-32insCTAG	XP_016867154.1:n.-4-33_-4-32insCTAG
XR_001744525.2:n.1020-33_1020-32insCTAG
XR_002956405.1:n.1162-33_1162-32insCTAG
NM_014251.3:c.849-33_849-32insCTAG MANE Select	NP_055066.1:n.849-33_849-32insCTAG
NR_027662.2:n.875-33_875-32insCTAG
NM_001160210.2:c.849-33_849-32insCTAG	NP_001153682.1:n.849-33_849-32insCTAG