Canonical Allele Identifier: CA2578945905

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96169965-AGTCCACACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96169968_96169977del , CM000669.2:g.96169968_96169977del	GRCh38
NC_000007.13:g.95799280_95799289del , CM000669.1:g.95799280_95799289del	GRCh37
NC_000007.12:g.95637216_95637225del	NCBI36
NG_012247.1:g.157173_157182del
NG_012247.2:g.157173_157182del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1311+70_1311+79del MANE Select	ENSP00000265631.6:n.1311+70_1311+79del
ENST00000265631.9:c.1311+70_1311+79del	ENSP00000265631.5:n.1311+70_1311+79del
ENST00000416240.6:c.1314+70_1314+79del	ENSP00000400101.2:n.1314+70_1314+79del
ENST00000484495.5:n.465-32_465-23del
ENST00000490072.5:n.378+70_378+79del
NM_001160210.1:c.1314+70_1314+79del	NP_001153682.1:n.1314+70_1314+79del
NM_014251.2:c.1311+70_1311+79del	NP_055066.1:n.1311+70_1311+79del
NR_027662.1:n.1386+70_1386+79del
XM_006715831.2:c.1344+70_1344+79del	XP_006715894.1:n.1344+70_1344+79del
XM_011515727.1:c.1345-32_1345-23del	XP_011514029.1:n.1345-32_1345-23del
XM_011515728.1:c.459+70_459+79del	XP_011514030.1:n.459+70_459+79del
XM_006715831.4:c.1344+70_1344+79del	XP_006715894.1:n.1344+70_1344+79del
XM_011515727.3:c.1345-32_1345-23del	XP_011514029.1:n.1345-32_1345-23del
XM_017011663.1:c.1302+70_1302+79del	XP_016867152.1:n.1302+70_1302+79del
XM_017011664.2:c.459+70_459+79del	XP_016867153.1:n.459+70_459+79del
XM_017011665.1:c.459+70_459+79del	XP_016867154.1:n.459+70_459+79del
XR_001744525.2:n.1483-32_1483-23del
XR_002956405.1:n.2115+70_2115+79del
NM_014251.3:c.1311+70_1311+79del MANE Select	NP_055066.1:n.1311+70_1311+79del
NR_027662.2:n.1337+70_1337+79del
NM_001160210.2:c.1314+70_1314+79del	NP_001153682.1:n.1314+70_1314+79del