Canonical Allele Identifier: CA2395758473
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176932T= , CM000684.2:g.19176932T= GRCh38
NC_000022.10:g.19164445T= , CM000684.1:g.19164445T= GRCh37
NC_000022.9:g.17544445T= NCBI36
NG_033863.1:g.6932A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.545A= MANE Select ENSP00000215882.5:p.Gln182=
ENST00000215882.9:c.545A= ENSP00000215882.5:p.Gln182=
ENST00000451283.5:c.236A= ENSP00000401480.1:p.Gln79=
ENST00000461267.1:n.691A=
ENST00000470922.5:n.687A=
NM_001256534.1:c.566A= NP_001243463.1:p.Gln189=
NM_001287387.1:c.236A= NP_001274316.1:p.Gln79=
NM_005984.4:c.545A= NP_005975.1:p.Gln182=
NR_046298.2:n.596A=
NM_005984.5:c.545A= MANE Select NP_005975.1:p.Gln182=
NM_001256534.2:c.566A= NP_001243463.1:p.Gln189=
NM_001287387.2:c.236A= NP_001274316.1:p.Gln79=
NR_046298.3:n.469A=