Linked Data
MyVariant Identifiers:
chr7:g.37927897G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37888295G>T , CM000669.2:g.37888295G>T | GRCh38 |
| NC_000007.13:g.37927897G>T , CM000669.1:g.37927897G>T | GRCh37 |
| NC_000007.12:g.37894422G>T | NCBI36 |
| NG_015893.1:g.44699G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000199447.9:c.1266G>T (NME8) MANE Select | ENSP00000199447.4:p.Ala422= | |
| ENST00000199447.8:c.1266G>T (NME8) | ENSP00000199447.4:p.Ala422= | |
| ENST00000426106.1:c.*212G>T (NME8) | ENSP00000408841.1:n.*212G>T | |
| ENST00000440017.5:c.1266G>T (NME8) | ENSP00000397063.1:p.Ala422= | |
| ENST00000476620.1:c.-38+30950G>T (EPDR1) | ENSP00000425858.1:n.-38+30950G>T | |
| NM_016616.4:c.1266G>T (NME8) | NP_057700.3:p.Ala422= | |
| NM_016616.5:c.1266G>T (NME8) MANE Select | NP_057700.3:p.Ala422= |