Canonical Allele Identifier: CA321344061
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1033601232

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176490A>G , CM000684.2:g.19176490A>G GRCh38
NC_000022.10:g.19164003A>G , CM000684.1:g.19164003A>G GRCh37
NC_000022.9:g.17544003A>G NCBI36
NG_033863.1:g.7374T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.752T>C MANE Select ENSP00000215882.5:p.Leu251Pro
ENST00000215882.9:c.752T>C ENSP00000215882.5:p.Leu251Pro
ENST00000451283.5:c.443T>C ENSP00000401480.1:p.Leu148Pro
ENST00000470922.5:n.894T>C
NM_001256534.1:c.773T>C NP_001243463.1:p.Leu258Pro
NM_001287387.1:c.443T>C NP_001274316.1:p.Leu148Pro
NM_005984.4:c.752T>C NP_005975.1:p.Leu251Pro
NR_046298.2:n.803T>C
NM_005984.5:c.752T>C MANE Select NP_005975.1:p.Leu251Pro
NM_001256534.2:c.773T>C NP_001243463.1:p.Leu258Pro
NM_001287387.2:c.443T>C NP_001274316.1:p.Leu148Pro
NR_046298.3:n.676T>C