Canonical Allele Identifier: CA410633801
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs2083956926

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176191A>G , CM000684.2:g.19176191A>G GRCh38
NC_000022.10:g.19163704A>G , CM000684.1:g.19163704A>G GRCh37
NC_000022.9:g.17543704A>G NCBI36
NG_033863.1:g.7673T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.875T>C MANE Select ENSP00000215882.5:p.Ile292Thr
ENST00000215882.9:c.875T>C ENSP00000215882.5:p.Ile292Thr
ENST00000451283.5:c.566T>C ENSP00000401480.1:p.Ile189Thr
ENST00000470922.5:n.1017T>C
NM_001256534.1:c.896T>C NP_001243463.1:p.Ile299Thr
NM_001287387.1:c.566T>C NP_001274316.1:p.Ile189Thr
NM_005984.4:c.875T>C NP_005975.1:p.Ile292Thr
NR_046298.2:n.926T>C
NM_005984.5:c.875T>C MANE Select NP_005975.1:p.Ile292Thr
NM_001256534.2:c.896T>C NP_001243463.1:p.Ile299Thr
NM_001287387.2:c.566T>C NP_001274316.1:p.Ile189Thr
NR_046298.3:n.799T>C