Linked Data
dbSNP Id:
rs757194964
gnomAD v2:
2-29420634-CT-C
gnomAD v3:
2-29197768-CT-C
gnomAD v4:
2-29197768-CT-C
COSMIC:
COSN18726320
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29197775del , CM000664.2:g.29197775del | GRCh38 |
| NC_000002.11:g.29420641del , CM000664.1:g.29420641del | GRCh37 |
| NC_000002.10:g.29274145del | NCBI36 |
| NG_009445.1:g.728798del , LRG_488:g.728798del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689605.1:c.*769del (CLIP4) | ENSP00000508948.1:n.*769del | |
| ENST00000389048.8:c.3939-93del (ALK) MANE Select | ENSP00000373700.3:n.3939-93del | |
| ENST00000431873.6:c.1166-93del (ALK) | ||
| ENST00000638605.1:n.816-93del (ALK) | ||
| ENST00000642122.1:c.735-93del (ALK) | ENSP00000493203.1:n.735-93del | |
| ENST00000389048.7:c.3939-93del (ALK) | ENSP00000373700.3:n.3939-93del | |
| ENST00000431873.5:c.819-93del (ALK) | ENSP00000414027.2:n.819-93del | |
| ENST00000618119.4:c.2808-93del (ALK) | ENSP00000482733.1:n.2808-93del | |
| NM_004304.4:c.3939-93del (ALK) | NP_004295.2:n.3939-93del | |
| NM_001353765.1:c.735-93del (ALK) | NP_001340694.1:n.735-93del | |
| XM_024452778.1:c.1092-93del (ALK) | XP_024308546.1:n.1092-93del | |
| XM_024452779.1:c.735-93del (ALK) | XP_024308547.1:n.735-93del | |
| NM_004304.5:c.3939-93del (ALK) MANE Select | NP_004295.2:n.3939-93del | |
| NM_001353765.2:c.735-93del (ALK) | NP_001340694.1:n.735-93del |