Canonical Allele Identifier: CA2395757915
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176198C= , CM000684.2:g.19176198C= GRCh38
NC_000022.10:g.19163711C= , CM000684.1:g.19163711C= GRCh37
NC_000022.9:g.17543711C= NCBI36
NG_033863.1:g.7666G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.868G= MANE Select ENSP00000215882.5:p.Val290=
ENST00000215882.9:c.868G= ENSP00000215882.5:p.Val290=
ENST00000451283.5:c.559G= ENSP00000401480.1:p.Val187=
ENST00000470922.5:n.1010G=
NM_001256534.1:c.889G= NP_001243463.1:p.Val297=
NM_001287387.1:c.559G= NP_001274316.1:p.Val187=
NM_005984.4:c.868G= NP_005975.1:p.Val290=
NR_046298.2:n.919G=
NM_005984.5:c.868G= MANE Select NP_005975.1:p.Val290=
NM_001256534.2:c.889G= NP_001243463.1:p.Val297=
NM_001287387.2:c.559G= NP_001274316.1:p.Val187=
NR_046298.3:n.792G=