Canonical Allele Identifier: CA2395758422
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs2083968231

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176823G>C , CM000684.2:g.19176823G>C GRCh38
NC_000022.10:g.19164336G>C , CM000684.1:g.19164336G>C GRCh37
NC_000022.9:g.17544336G>C NCBI36
NG_033863.1:g.7041C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.631+23C>G MANE Select ENSP00000215882.5:n.631+23C>G
ENST00000215882.9:c.631+23C>G ENSP00000215882.5:n.631+23C>G
ENST00000451283.5:c.322+23C>G ENSP00000401480.1:n.322+23C>G
ENST00000461267.1:n.777+23C>G
ENST00000470922.5:n.773+23C>G
NM_001256534.1:c.652+23C>G NP_001243463.1:n.652+23C>G
NM_001287387.1:c.322+23C>G NP_001274316.1:n.322+23C>G
NM_005984.4:c.631+23C>G NP_005975.1:n.631+23C>G
NR_046298.2:n.682+23C>G
NM_005984.5:c.631+23C>G MANE Select NP_005975.1:n.631+23C>G
NM_001256534.2:c.652+23C>G NP_001243463.1:n.652+23C>G
NM_001287387.2:c.322+23C>G NP_001274316.1:n.322+23C>G
NR_046298.3:n.555+23C>G