Canonical Allele Identifier: CA410634536
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs2083960955

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176458A>G , CM000684.2:g.19176458A>G GRCh38
NC_000022.10:g.19163971A>G , CM000684.1:g.19163971A>G GRCh37
NC_000022.9:g.17543971A>G NCBI36
NG_033863.1:g.7406T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.784T>C MANE Select ENSP00000215882.5:p.Cys262Arg
ENST00000215882.9:c.784T>C ENSP00000215882.5:p.Cys262Arg
ENST00000451283.5:c.475T>C ENSP00000401480.1:p.Cys159Arg
ENST00000470922.5:n.926T>C
NM_001256534.1:c.805T>C NP_001243463.1:p.Cys269Arg
NM_001287387.1:c.475T>C NP_001274316.1:p.Cys159Arg
NM_005984.4:c.784T>C NP_005975.1:p.Cys262Arg
NR_046298.2:n.835T>C
NM_005984.5:c.784T>C MANE Select NP_005975.1:p.Cys262Arg
NM_001256534.2:c.805T>C NP_001243463.1:p.Cys269Arg
NM_001287387.2:c.475T>C NP_001274316.1:p.Cys159Arg
NR_046298.3:n.708T>C