Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143502144T= , CM000668.2:g.143502144T= | GRCh38 |
| NC_000006.11:g.143823281T= , CM000668.1:g.143823281T= | GRCh37 |
| NC_000006.10:g.143864974T= | NCBI36 |
| NG_027676.1:g.14740A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032020.5:c.964-22A= (FUCA2) MANE Select | NP_114409.2:n.964-22A= |
| ENST00000002165.11:c.964-22A= (FUCA2) MANE Select | ENSP00000002165.5:n.964-22A= |
| NM_032020.4:c.964-22A= (FUCA2) | NP_114409.2:n.964-22A= |
| ENST00000002165.10:c.964-22A= (FUCA2) | ENSP00000002165.5:n.964-22A= |
| ENST00000367585.1:n.469-22A= (FUCA2) | |
| ENST00000438118.6:n.801-1250T= (VDAC1P8) | |
| ENST00000589563.5:n.502-3196T= (VDAC1P8) | |
| ENST00000610068.5:n.969-1250T= (VDAC1P8) | |
| ENST00000622321.1:n.91-1250T= (VDAC1P8) |