Canonical Allele Identifier: CA410636630
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176666G>C , CM000684.2:g.19176666G>C GRCh38
NC_000022.10:g.19164179G>C , CM000684.1:g.19164179G>C GRCh37
NC_000022.9:g.17544179G>C NCBI36
NG_033863.1:g.7198C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.659C>G MANE Select ENSP00000215882.5:p.Pro220Arg
ENST00000215882.9:c.659C>G ENSP00000215882.5:p.Pro220Arg
ENST00000451283.5:c.350C>G ENSP00000401480.1:p.Pro117Arg
ENST00000470922.5:n.801C>G
NM_001256534.1:c.680C>G NP_001243463.1:p.Pro227Arg
NM_001287387.1:c.350C>G NP_001274316.1:p.Pro117Arg
NM_005984.4:c.659C>G NP_005975.1:p.Pro220Arg
NR_046298.2:n.710C>G
NM_005984.5:c.659C>G MANE Select NP_005975.1:p.Pro220Arg
NM_001256534.2:c.680C>G NP_001243463.1:p.Pro227Arg
NM_001287387.2:c.350C>G NP_001274316.1:p.Pro117Arg
NR_046298.3:n.583C>G