Canonical Allele Identifier: CA2395758359
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1418586184

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176719T>G , CM000684.2:g.19176719T>G GRCh38
NC_000022.10:g.19164232T>G , CM000684.1:g.19164232T>G GRCh37
NC_000022.9:g.17544232T>G NCBI36
NG_033863.1:g.7145A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.632-26A>C MANE Select ENSP00000215882.5:n.632-26A>C
ENST00000215882.9:c.632-26A>C ENSP00000215882.5:n.632-26A>C
ENST00000451283.5:c.323-26A>C ENSP00000401480.1:n.323-26A>C
ENST00000461267.1:n.778-26A>C
ENST00000470922.5:n.774-26A>C
NM_001256534.1:c.653-26A>C NP_001243463.1:n.653-26A>C
NM_001287387.1:c.323-26A>C NP_001274316.1:n.323-26A>C
NM_005984.4:c.632-26A>C NP_005975.1:n.632-26A>C
NR_046298.2:n.683-26A>C
NM_005984.5:c.632-26A>C MANE Select NP_005975.1:n.632-26A>C
NM_001256534.2:c.653-26A>C NP_001243463.1:n.653-26A>C
NM_001287387.2:c.323-26A>C NP_001274316.1:n.323-26A>C
NR_046298.3:n.556-26A>C