Canonical Allele Identifier: CA2395757873
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176109C= , CM000684.2:g.19176109C= GRCh38
NC_000022.10:g.19163622C= , CM000684.1:g.19163622C= GRCh37
NC_000022.9:g.17543622C= NCBI36
NG_033863.1:g.7755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*21G= MANE Select ENSP00000215882.5:n.*21G=
ENST00000215882.9:c.*21G= ENSP00000215882.5:n.*21G=
ENST00000451283.5:c.*21G= ENSP00000401480.1:n.*21G=
ENST00000470922.5:n.1099G=
NM_001256534.1:c.*21G= NP_001243463.1:n.*21G=
NM_001287387.1:c.*21G= NP_001274316.1:n.*21G=
NM_005984.4:c.*21G= NP_005975.1:n.*21G=
NR_046298.2:n.1008G=
NM_005984.5:c.*21G= MANE Select NP_005975.1:n.*21G=
NM_001256534.2:c.*21G= NP_001243463.1:n.*21G=
NM_001287387.2:c.*21G= NP_001274316.1:n.*21G=
NR_046298.3:n.881G=