Canonical Allele Identifier: CA2655261354
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1386039617

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176257A>C , CM000684.2:g.19176257A>C GRCh38
NC_000022.10:g.19163770A>C , CM000684.1:g.19163770A>C GRCh37
NC_000022.9:g.17543770A>C NCBI36
NG_033863.1:g.7607T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.822-13T>G MANE Select ENSP00000215882.5:n.822-13T>G
ENST00000215882.9:c.822-13T>G ENSP00000215882.5:n.822-13T>G
ENST00000451283.5:c.513-13T>G ENSP00000401480.1:n.513-13T>G
ENST00000470922.5:n.964-13T>G
NM_001256534.1:c.843-13T>G NP_001243463.1:n.843-13T>G
NM_001287387.1:c.513-13T>G NP_001274316.1:n.513-13T>G
NM_005984.4:c.822-13T>G NP_005975.1:n.822-13T>G
NR_046298.2:n.873-13T>G
NM_005984.5:c.822-13T>G MANE Select NP_005975.1:n.822-13T>G
NM_001256534.2:c.843-13T>G NP_001243463.1:n.843-13T>G
NM_001287387.2:c.513-13T>G NP_001274316.1:n.513-13T>G
NR_046298.3:n.746-13T>G