Canonical Allele Identifier: CA2655261337
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176126A>G , CM000684.2:g.19176126A>G GRCh38
NC_000022.10:g.19163639A>G , CM000684.1:g.19163639A>G GRCh37
NC_000022.9:g.17543639A>G NCBI36
NG_033863.1:g.7738T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*4T>C MANE Select ENSP00000215882.5:n.*4T>C
ENST00000215882.9:c.*4T>C ENSP00000215882.5:n.*4T>C
ENST00000451283.5:c.*4T>C ENSP00000401480.1:n.*4T>C
ENST00000470922.5:n.1082T>C
NM_001256534.1:c.*4T>C NP_001243463.1:n.*4T>C
NM_001287387.1:c.*4T>C NP_001274316.1:n.*4T>C
NM_005984.4:c.*4T>C NP_005975.1:n.*4T>C
NR_046298.2:n.991T>C
NM_005984.5:c.*4T>C MANE Select NP_005975.1:n.*4T>C
NM_001256534.2:c.*4T>C NP_001243463.1:n.*4T>C
NM_001287387.2:c.*4T>C NP_001274316.1:n.*4T>C
NR_046298.3:n.864T>C