Canonical Allele Identifier: CA2655261526
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176954_19176955del , CM000684.2:g.19176954_19176955del GRCh38
NC_000022.10:g.19164467_19164468del , CM000684.1:g.19164467_19164468del GRCh37
NC_000022.9:g.17544467_17544468del NCBI36
NG_033863.1:g.6910_6911del

Transcript Alleles

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