Canonical Allele Identifier: CA2683825448

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189389-AAAACAAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189391_96189398del , CM000669.2:g.96189391_96189398del	GRCh38
NC_000007.13:g.95818703_95818710del , CM000669.1:g.95818703_95818710del	GRCh37
NC_000007.12:g.95656639_95656646del	NCBI36
NG_012247.1:g.137751_137758del
NG_012247.2:g.137751_137758del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-19_849-12del MANE Select	ENSP00000265631.6:n.849-19_849-12del
ENST00000265631.9:c.849-19_849-12del	ENSP00000265631.5:n.849-19_849-12del
ENST00000416240.6:c.849-19_849-12del	ENSP00000400101.2:n.849-19_849-12del
NM_001160210.1:c.849-19_849-12del	NP_001153682.1:n.849-19_849-12del
NM_014251.2:c.849-19_849-12del	NP_055066.1:n.849-19_849-12del
NR_027662.1:n.924-19_924-12del
XM_006715831.2:c.882-19_882-12del	XP_006715894.1:n.882-19_882-12del
XM_011515727.1:c.882-19_882-12del	XP_011514029.1:n.882-19_882-12del
XM_011515728.1:c.-4-19_-4-12del	XP_011514030.1:n.-4-19_-4-12del
XM_006715831.4:c.882-19_882-12del	XP_006715894.1:n.882-19_882-12del
XM_011515727.3:c.882-19_882-12del	XP_011514029.1:n.882-19_882-12del
XM_017011663.1:c.840-19_840-12del	XP_016867152.1:n.840-19_840-12del
XM_017011664.2:c.-4-19_-4-12del	XP_016867153.1:n.-4-19_-4-12del
XM_017011665.1:c.-4-19_-4-12del	XP_016867154.1:n.-4-19_-4-12del
XR_001744525.2:n.1020-19_1020-12del
XR_002956405.1:n.1162-19_1162-12del
NM_014251.3:c.849-19_849-12del MANE Select	NP_055066.1:n.849-19_849-12del
NR_027662.2:n.875-19_875-12del
NM_001160210.2:c.849-19_849-12del	NP_001153682.1:n.849-19_849-12del