Canonical Allele Identifier: CA2395758529

Gene: SLC25A1

Linked Data

• dbSNP Id: rs2083971991

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177003_19177009del , CM000684.2:g.19177003_19177009del	GRCh38
NC_000022.10:g.19164516_19164522del , CM000684.1:g.19164516_19164522del	GRCh37
NC_000022.9:g.17544516_17544522del	NCBI36
NG_033863.1:g.6859_6865del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.527-55_527-49del MANE Select	ENSP00000215882.5:n.527-55_527-49del
ENST00000215882.9:c.527-55_527-49del	ENSP00000215882.5:n.527-55_527-49del
ENST00000451283.5:c.218-55_218-49del	ENSP00000401480.1:n.218-55_218-49del
ENST00000461267.1:n.673-55_673-49del
ENST00000470922.5:n.669-55_669-49del
NM_001256534.1:c.548-55_548-49del	NP_001243463.1:n.548-55_548-49del
NM_001287387.1:c.218-55_218-49del	NP_001274316.1:n.218-55_218-49del
NM_005984.4:c.527-55_527-49del	NP_005975.1:n.527-55_527-49del
NR_046298.2:n.578-55_578-49del
NM_005984.5:c.527-55_527-49del MANE Select	NP_005975.1:n.527-55_527-49del
NM_001256534.2:c.548-55_548-49del	NP_001243463.1:n.548-55_548-49del
NM_001287387.2:c.218-55_218-49del	NP_001274316.1:n.218-55_218-49del
NR_046298.3:n.451-55_451-49del