Canonical Allele Identifier: CA2395758498
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs372319041

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176968C>G , CM000684.2:g.19176968C>G GRCh38
NC_000022.10:g.19164481C>G , CM000684.1:g.19164481C>G GRCh37
NC_000022.9:g.17544481C>G NCBI36
NG_033863.1:g.6896G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.527-18G>C MANE Select ENSP00000215882.5:n.527-18G>C
ENST00000215882.9:c.527-18G>C ENSP00000215882.5:n.527-18G>C
ENST00000451283.5:c.218-18G>C ENSP00000401480.1:n.218-18G>C
ENST00000461267.1:n.673-18G>C
ENST00000470922.5:n.669-18G>C
NM_001256534.1:c.548-18G>C NP_001243463.1:n.548-18G>C
NM_001287387.1:c.218-18G>C NP_001274316.1:n.218-18G>C
NM_005984.4:c.527-18G>C NP_005975.1:n.527-18G>C
NR_046298.2:n.578-18G>C
NM_005984.5:c.527-18G>C MANE Select NP_005975.1:n.527-18G>C
NM_001256534.2:c.548-18G>C NP_001243463.1:n.548-18G>C
NM_001287387.2:c.218-18G>C NP_001274316.1:n.218-18G>C
NR_046298.3:n.451-18G>C