Canonical Allele Identifier: CA2395758822
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177768C= , CM000684.2:g.19177768C= GRCh38
NC_000022.10:g.19165281C= , CM000684.1:g.19165281C= GRCh37
NC_000022.9:g.17545281C= NCBI36
NG_033805.1:g.118949G=
NG_033863.1:g.6096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.400G= MANE Select ENSP00000215882.5:p.Ala134=
ENST00000215882.9:c.400G= ENSP00000215882.5:p.Ala134=
ENST00000451283.5:c.91G= ENSP00000401480.1:p.Ala31=
ENST00000461267.1:n.546G=
ENST00000470922.5:n.542G=
NM_001256534.1:c.421G= NP_001243463.1:p.Ala141=
NM_001287387.1:c.91G= NP_001274316.1:p.Ala31=
NM_005984.4:c.400G= NP_005975.1:p.Ala134=
NR_046298.2:n.492+174G=
NM_005984.5:c.400G= MANE Select NP_005975.1:p.Ala134=
NM_001256534.2:c.421G= NP_001243463.1:p.Ala141=
NM_001287387.2:c.91G= NP_001274316.1:p.Ala31=
NR_046298.3:n.365+174G=