Canonical Allele Identifier: CA10097380
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs374948045

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176885G>A , CM000684.2:g.19176885G>A GRCh38
NC_000022.10:g.19164398G>A , CM000684.1:g.19164398G>A GRCh37
NC_000022.9:g.17544398G>A NCBI36
NG_033863.1:g.6979C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.592C>T MANE Select ENSP00000215882.5:p.Arg198Cys
ENST00000215882.9:c.592C>T ENSP00000215882.5:p.Arg198Cys
ENST00000451283.5:c.283C>T ENSP00000401480.1:p.Arg95Cys
ENST00000461267.1:n.738C>T
ENST00000470922.5:n.734C>T
NM_001256534.1:c.613C>T NP_001243463.1:p.Arg205Cys
NM_001287387.1:c.283C>T NP_001274316.1:p.Arg95Cys
NM_005984.4:c.592C>T NP_005975.1:p.Arg198Cys
NR_046298.2:n.643C>T
NM_005984.5:c.592C>T MANE Select NP_005975.1:p.Arg198Cys
NM_001256534.2:c.613C>T NP_001243463.1:p.Arg205Cys
NM_001287387.2:c.283C>T NP_001274316.1:p.Arg95Cys
NR_046298.3:n.516C>T