Canonical Allele Identifier: CA2395758474
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176933G= , CM000684.2:g.19176933G= GRCh38
NC_000022.10:g.19164446G= , CM000684.1:g.19164446G= GRCh37
NC_000022.9:g.17544446G= NCBI36
NG_033863.1:g.6931C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.544C= MANE Select ENSP00000215882.5:p.Gln182=
ENST00000215882.9:c.544C= ENSP00000215882.5:p.Gln182=
ENST00000451283.5:c.235C= ENSP00000401480.1:p.Gln79=
ENST00000461267.1:n.690C=
ENST00000470922.5:n.686C=
NM_001256534.1:c.565C= NP_001243463.1:p.Gln189=
NM_001287387.1:c.235C= NP_001274316.1:p.Gln79=
NM_005984.4:c.544C= NP_005975.1:p.Gln182=
NR_046298.2:n.595C=
NM_005984.5:c.544C= MANE Select NP_005975.1:p.Gln182=
NM_001256534.2:c.565C= NP_001243463.1:p.Gln189=
NM_001287387.2:c.235C= NP_001274316.1:p.Gln79=
NR_046298.3:n.468C=