Canonical Allele Identifier: CA410636577
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176658T>G , CM000684.2:g.19176658T>G GRCh38
NC_000022.10:g.19164171T>G , CM000684.1:g.19164171T>G GRCh37
NC_000022.9:g.17544171T>G NCBI36
NG_033863.1:g.7206A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.667A>C MANE Select ENSP00000215882.5:p.Thr223Pro
ENST00000215882.9:c.667A>C ENSP00000215882.5:p.Thr223Pro
ENST00000451283.5:c.358A>C ENSP00000401480.1:p.Thr120Pro
ENST00000470922.5:n.809A>C
NM_001256534.1:c.688A>C NP_001243463.1:p.Thr230Pro
NM_001287387.1:c.358A>C NP_001274316.1:p.Thr120Pro
NM_005984.4:c.667A>C NP_005975.1:p.Thr223Pro
NR_046298.2:n.718A>C
NM_005984.5:c.667A>C MANE Select NP_005975.1:p.Thr223Pro
NM_001256534.2:c.688A>C NP_001243463.1:p.Thr230Pro
NM_001287387.2:c.358A>C NP_001274316.1:p.Thr120Pro
NR_046298.3:n.591A>C