Canonical Allele Identifier: CA2395758488
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1555922547

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176956G>T , CM000684.2:g.19176956G>T GRCh38
NC_000022.10:g.19164469G>T , CM000684.1:g.19164469G>T GRCh37
NC_000022.9:g.17544469G>T NCBI36
NG_033863.1:g.6908C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.527-6C>A MANE Select ENSP00000215882.5:n.527-6C>A
ENST00000215882.9:c.527-6C>A ENSP00000215882.5:n.527-6C>A
ENST00000451283.5:c.218-6C>A ENSP00000401480.1:n.218-6C>A
ENST00000461267.1:n.673-6C>A
ENST00000470922.5:n.669-6C>A
NM_001256534.1:c.548-6C>A NP_001243463.1:n.548-6C>A
NM_001287387.1:c.218-6C>A NP_001274316.1:n.218-6C>A
NM_005984.4:c.527-6C>A NP_005975.1:n.527-6C>A
NR_046298.2:n.578-6C>A
NM_005984.5:c.527-6C>A MANE Select NP_005975.1:n.527-6C>A
NM_001256534.2:c.548-6C>A NP_001243463.1:n.548-6C>A
NM_001287387.2:c.218-6C>A NP_001274316.1:n.218-6C>A
NR_046298.3:n.451-6C>A