Canonical Allele Identifier: CA10097374
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs557032951

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176861G>A , CM000684.2:g.19176861G>A GRCh38
NC_000022.10:g.19164374G>A , CM000684.1:g.19164374G>A GRCh37
NC_000022.9:g.17544374G>A NCBI36
NG_033863.1:g.7003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.616C>T MANE Select ENSP00000215882.5:p.Arg206Cys
ENST00000215882.9:c.616C>T ENSP00000215882.5:p.Arg206Cys
ENST00000451283.5:c.307C>T ENSP00000401480.1:p.Arg103Cys
ENST00000461267.1:n.762C>T
ENST00000470922.5:n.758C>T
NM_001256534.1:c.637C>T NP_001243463.1:p.Arg213Cys
NM_001287387.1:c.307C>T NP_001274316.1:p.Arg103Cys
NM_005984.4:c.616C>T NP_005975.1:p.Arg206Cys
NR_046298.2:n.667C>T
NM_005984.5:c.616C>T MANE Select NP_005975.1:p.Arg206Cys
NM_001256534.2:c.637C>T NP_001243463.1:p.Arg213Cys
NM_001287387.2:c.307C>T NP_001274316.1:p.Arg103Cys
NR_046298.3:n.540C>T