Canonical Allele Identifier: CA410635816
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176578C>A , CM000684.2:g.19176578C>A GRCh38
NC_000022.10:g.19164091C>A , CM000684.1:g.19164091C>A GRCh37
NC_000022.9:g.17544091C>A NCBI36
NG_033863.1:g.7286G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.747G>T MANE Select ENSP00000215882.5:p.Gln249His
ENST00000215882.9:c.747G>T ENSP00000215882.5:p.Gln249His
ENST00000451283.5:c.438G>T ENSP00000401480.1:p.Gln146His
ENST00000470922.5:n.889G>T
NM_001256534.1:c.768G>T NP_001243463.1:p.Gln256His
NM_001287387.1:c.438G>T NP_001274316.1:p.Gln146His
NM_005984.4:c.747G>T NP_005975.1:p.Gln249His
NR_046298.2:n.798G>T
NM_005984.5:c.747G>T MANE Select NP_005975.1:p.Gln249His
NM_001256534.2:c.768G>T NP_001243463.1:p.Gln256His
NM_001287387.2:c.438G>T NP_001274316.1:p.Gln146His
NR_046298.3:n.671G>T