Linked Data
ClinVar Variation Id:
133479
dbSNP Id:
rs56181542
ExAC:
2:29416698 C / T
gnomAD v2:
2-29416698-C-T
gnomAD v3:
2-29193832-C-T
gnomAD v4:
2-29193832-C-T
COSMIC:
COSM159021
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29193832C>T , CM000664.2:g.29193832C>T | GRCh38 |
| NC_000002.11:g.29416698C>T , CM000664.1:g.29416698C>T | GRCh37 |
| NC_000002.10:g.29270202C>T | NCBI36 |
| NG_009445.1:g.732735G>A , LRG_488:g.732735G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689605.1:c.1923-3096C>T (CLIP4) | ENSP00000508948.1:n.1923-3096C>T | |
| ENST00000389048.8:c.4255G>A (ALK) MANE Select | ENSP00000373700.3:p.Glu1419Lys | |
| ENST00000431873.6:c.1482G>A (ALK) | ||
| ENST00000638605.1:n.1132G>A (ALK) | ||
| ENST00000642122.1:c.1051G>A (ALK) | ENSP00000493203.1:p.Glu351Lys | |
| ENST00000389048.7:c.4255G>A (ALK) | ENSP00000373700.3:p.Glu1419Lys | |
| ENST00000431873.5:c.1135G>A (ALK) | ENSP00000414027.2:p.Glu379Lys | |
| ENST00000618119.4:c.3124G>A (ALK) | ENSP00000482733.1:p.Glu1042Lys | |
| NM_004304.4:c.4255G>A (ALK) | NP_004295.2:p.Glu1419Lys | |
| NM_001353765.1:c.1051G>A (ALK) | NP_001340694.1:p.Glu351Lys | |
| XM_024452778.1:c.1408G>A (ALK) | XP_024308546.1:p.Glu470Lys | |
| XM_024452779.1:c.1051G>A (ALK) | XP_024308547.1:p.Glu351Lys | |
| NM_004304.5:c.4255G>A (ALK) MANE Select | NP_004295.2:p.Glu1419Lys | |
| NM_001353765.2:c.1051G>A (ALK) | NP_001340694.1:p.Glu351Lys |