Canonical Allele Identifier: CA2395758039
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176444G= , CM000684.2:g.19176444G= GRCh38
NC_000022.10:g.19163957G= , CM000684.1:g.19163957G= GRCh37
NC_000022.9:g.17543957G= NCBI36
NG_033863.1:g.7420C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.798C= MANE Select ENSP00000215882.5:p.Ile266=
ENST00000215882.9:c.798C= ENSP00000215882.5:p.Ile266=
ENST00000451283.5:c.489C= ENSP00000401480.1:p.Ile163=
ENST00000470922.5:n.940C=
NM_001256534.1:c.819C= NP_001243463.1:p.Ile273=
NM_001287387.1:c.489C= NP_001274316.1:p.Ile163=
NM_005984.4:c.798C= NP_005975.1:p.Ile266=
NR_046298.2:n.849C=
NM_005984.5:c.798C= MANE Select NP_005975.1:p.Ile266=
NM_001256534.2:c.819C= NP_001243463.1:p.Ile273=
NM_001287387.2:c.489C= NP_001274316.1:p.Ile163=
NR_046298.3:n.722C=