Linked Data
ClinVar Variation Id:
38403
ClinVar RCV Id:
RCV000031955
dbSNP Id:
rs202247807
gnomAD v2:
13-41383720-C-T
gnomAD v3:
13-40809584-C-T
gnomAD v4:
13-40809584-C-T
PubMed:
PMID:22649802
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.40809584C>T , CM000675.2:g.40809584C>T | GRCh38 |
| NC_000013.10:g.41383720C>T , CM000675.1:g.41383720C>T | GRCh37 |
| NC_000013.9:g.40281720C>T | NCBI36 |
| NG_012248.1:g.25174C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000707033.1:c.823C>T (SLC25A15) | ENSP00000516711.1:p.Arg275Ter | |
| ENST00000338625.9:c.823C>T (SLC25A15) MANE Select | ENSP00000342267.4:p.Arg275Ter | |
| ENST00000338625.8:c.823C>T (SLC25A15) | ENSP00000342267.4:p.Arg275Ter | |
| NM_014252.3:c.823C>T (SLC25A15) | NP_055067.1:p.Arg275Ter | |
| NR_038258.1:n.623-8860G>A (TPTE2P5) | ||
| NR_038259.1:n.452-8860G>A (TPTE2P5) | ||
| NM_014252.4:c.823C>T (SLC25A15) MANE Select | NP_055067.1:p.Arg275Ter |