Linked Data
ClinVar Variation Id:
404328
dbSNP Id:
rs376702277
ExAC:
2:29416152 C / T
gnomAD v2:
2-29416152-C-T
gnomAD v3:
2-29193286-C-T
gnomAD v4:
2-29193286-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29193286C>T , CM000664.2:g.29193286C>T | GRCh38 |
| NC_000002.11:g.29416152C>T , CM000664.1:g.29416152C>T | GRCh37 |
| NC_000002.10:g.29269656C>T | NCBI36 |
| NG_009445.1:g.733281G>A , LRG_488:g.733281G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689605.1:c.1923-3642C>T (CLIP4) | ENSP00000508948.1:n.1923-3642C>T | |
| ENST00000389048.8:c.4801G>A (ALK) MANE Select | ENSP00000373700.3:p.Ala1601Thr | |
| ENST00000431873.6:c.2028G>A (ALK) | ||
| ENST00000638605.1:n.1678G>A (ALK) | ||
| ENST00000642122.1:c.1597G>A (ALK) | ENSP00000493203.1:p.Ala533Thr | |
| ENST00000389048.7:c.4801G>A (ALK) | ENSP00000373700.3:p.Ala1601Thr | |
| ENST00000431873.5:c.1681G>A (ALK) | ENSP00000414027.2:p.Ala561Thr | |
| ENST00000618119.4:c.3670G>A (ALK) | ENSP00000482733.1:p.Ala1224Thr | |
| NM_004304.4:c.4801G>A (ALK) | NP_004295.2:p.Ala1601Thr | |
| NM_001353765.1:c.1597G>A (ALK) | NP_001340694.1:p.Ala533Thr | |
| XM_024452778.1:c.1954G>A (ALK) | XP_024308546.1:p.Ala652Thr | |
| XM_024452779.1:c.1597G>A (ALK) | XP_024308547.1:p.Ala533Thr | |
| NM_004304.5:c.4801G>A (ALK) MANE Select | NP_004295.2:p.Ala1601Thr | |
| NM_001353765.2:c.1597G>A (ALK) | NP_001340694.1:p.Ala533Thr |