Canonical Allele Identifier: CA2395757886
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176127G= , CM000684.2:g.19176127G= GRCh38
NC_000022.10:g.19163640G= , CM000684.1:g.19163640G= GRCh37
NC_000022.9:g.17543640G= NCBI36
NG_033863.1:g.7737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*3C= MANE Select ENSP00000215882.5:n.*3C=
ENST00000215882.9:c.*3C= ENSP00000215882.5:n.*3C=
ENST00000451283.5:c.*3C= ENSP00000401480.1:n.*3C=
ENST00000470922.5:n.1081C=
NM_001256534.1:c.*3C= NP_001243463.1:n.*3C=
NM_001287387.1:c.*3C= NP_001274316.1:n.*3C=
NM_005984.4:c.*3C= NP_005975.1:n.*3C=
NR_046298.2:n.990C=
NM_005984.5:c.*3C= MANE Select NP_005975.1:n.*3C=
NM_001256534.2:c.*3C= NP_001243463.1:n.*3C=
NM_001287387.2:c.*3C= NP_001274316.1:n.*3C=
NR_046298.3:n.863C=