Linked Data
ClinVar Variation Id:
351315
ClinVar RCV Id:
RCV000316811
dbSNP Id:
rs772052566
gnomAD v2:
5-142657694-C-CT
gnomAD v3:
5-143278129-C-CT
gnomAD v4:
5-143278129-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.143278138dup , CM000667.2:g.143278138dup | GRCh38 |
| NC_000005.9:g.142657703dup , CM000667.1:g.142657703dup | GRCh37 |
| NC_000005.8:g.142637896dup | NCBI36 |
| NG_009062.1:g.162383dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394464.7:c.*3759dup MANE Select | ENSP00000377977.2:n.*3759dup | |
| ENST00000343796.6:c.*3759dup | ENSP00000343205.2:n.*3759dup | |
| ENST00000394464.6:c.*3759dup | ENSP00000377977.2:n.*3759dup | |
| ENST00000415690.6:c.*1234dup | ENSP00000387672.2:n.*1234dup | |
| NM_000176.2:c.*3759dup | NP_000167.1:n.*3759dup | |
| NM_001018074.1:c.*3759dup | NP_001018084.1:n.*3759dup | |
| NM_001018075.1:c.*3759dup | NP_001018085.1:n.*3759dup | |
| NM_001018076.1:c.*3759dup | NP_001018086.1:n.*3759dup | |
| NM_001018077.1:c.*3759dup | NP_001018087.1:n.*3759dup | |
| NM_001020825.1:c.*1234dup | NP_001018661.1:n.*1234dup | |
| NM_001024094.1:c.*3759dup | NP_001019265.1:n.*3759dup | |
| NM_001204258.1:c.*3759dup | NP_001191187.1:n.*3759dup | |
| NM_001204259.1:c.*3759dup | NP_001191188.1:n.*3759dup | |
| NM_001204260.1:c.*3759dup | NP_001191189.1:n.*3759dup | |
| NM_001204261.1:c.*3759dup | NP_001191190.1:n.*3759dup | |
| NM_001204262.1:c.*3759dup | NP_001191191.1:n.*3759dup | |
| NM_001204263.1:c.*3759dup | NP_001191192.1:n.*3759dup | |
| NM_001204264.1:c.*3759dup | NP_001191193.1:n.*3759dup | |
| XM_005268419.2:c.*3759dup | XP_005268476.1:n.*3759dup | |
| XM_005268420.3:c.*3759dup | XP_005268477.1:n.*3759dup | |
| XM_005268422.2:c.*3759dup | XP_005268479.1:n.*3759dup | |
| XM_005268423.2:c.*3759dup | XP_005268480.1:n.*3759dup | |
| XM_011537637.1:c.*3759dup | XP_011535939.1:n.*3759dup | |
| XR_944371.1:n.656-6561dup | ||
| NR_157096.1:n.5016dup | ||
| NM_000176.3:c.*3759dup MANE Select | NP_000167.1:n.*3759dup | |
| NM_001364180.1:c.*3759dup | NP_001351109.1:n.*3759dup | |
| NM_001364181.1:c.*3759dup | NP_001351110.1:n.*3759dup | |
| NM_001364182.1:c.*3759dup | NP_001351111.1:n.*3759dup | |
| NM_001364183.1:c.*3759dup | NP_001351112.1:n.*3759dup | |
| NM_001364184.1:c.*3759dup | NP_001351113.1:n.*3759dup | |
| NM_001364185.1:c.*3759dup | NP_001351114.1:n.*3759dup | |
| NM_001018076.2:c.*3759dup | NP_001018086.1:n.*3759dup | |
| NM_001020825.2:c.*1234dup | NP_001018661.1:n.*1234dup | |
| NM_001024094.2:c.*3759dup | NP_001019265.1:n.*3759dup | |
| NM_001204258.2:c.*3759dup | NP_001191187.1:n.*3759dup | |
| NM_001204259.2:c.*3759dup | NP_001191188.1:n.*3759dup | |
| NM_001204260.2:c.*3759dup | NP_001191189.1:n.*3759dup | |
| NM_001204261.2:c.*3759dup | NP_001191190.1:n.*3759dup | |
| NM_001204262.2:c.*3759dup | NP_001191191.1:n.*3759dup | |
| NM_001204263.2:c.*3759dup | NP_001191192.1:n.*3759dup | |
| NM_001204264.2:c.*3759dup | NP_001191193.1:n.*3759dup | |
| NM_001364180.2:c.*3759dup | NP_001351109.1:n.*3759dup | |
| NM_001364181.2:c.*3759dup | NP_001351110.1:n.*3759dup | |
| NM_001364183.2:c.*3759dup | NP_001351112.1:n.*3759dup | |
| NM_001364184.2:c.*3759dup | NP_001351113.1:n.*3759dup | |
| NR_157096.2:n.5016dup |