Linked Data
COSMIC:
COSM1442233
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.167341638_167341640del , CM000668.2:g.167341638_167341640del | GRCh38 |
| NC_000006.11:g.167755126_167755128del , CM000668.1:g.167755126_167755128del | GRCh37 |
| NC_000006.10:g.167675116_167675118del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239587.10:c.1738_1740del MANE Select | ENSP00000239587.5:p.Ile580del | |
| ENST00000649884.1:c.1519_1521del | ENSP00000497040.1:p.Ile507del | |
| ENST00000239587.9:c.1738_1740del | ENSP00000239587.5:p.Ile580del | |
| ENST00000515138.1:c.1738_1740del | ENSP00000424130.1:p.Ile580del | |
| NM_031949.4:c.1738_1740del | NP_114155.4:p.Ile580del | |
| XM_006715572.2:c.1519_1521del | XP_006715635.1:p.Ile507del | |
| XM_006715572.4:c.1519_1521del | XP_006715635.1:p.Ile507del | |
| NM_031949.5:c.1738_1740del MANE Select | NP_114155.4:p.Ile580del |