Canonical Allele Identifier: CA2655261332
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176120C>A , CM000684.2:g.19176120C>A GRCh38
NC_000022.10:g.19163633C>A , CM000684.1:g.19163633C>A GRCh37
NC_000022.9:g.17543633C>A NCBI36
NG_033863.1:g.7744G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*10G>T MANE Select ENSP00000215882.5:n.*10G>T
ENST00000215882.9:c.*10G>T ENSP00000215882.5:n.*10G>T
ENST00000451283.5:c.*10G>T ENSP00000401480.1:n.*10G>T
ENST00000470922.5:n.1088G>T
NM_001256534.1:c.*10G>T NP_001243463.1:n.*10G>T
NM_001287387.1:c.*10G>T NP_001274316.1:n.*10G>T
NM_005984.4:c.*10G>T NP_005975.1:n.*10G>T
NR_046298.2:n.997G>T
NM_005984.5:c.*10G>T MANE Select NP_005975.1:n.*10G>T
NM_001256534.2:c.*10G>T NP_001243463.1:n.*10G>T
NM_001287387.2:c.*10G>T NP_001274316.1:n.*10G>T
NR_046298.3:n.870G>T