Linked Data
ClinVar Variation Id:
1954945
ClinVar RCV Id:
RCV002690317
dbSNP Id:
rs2053871695
gnomAD v4:
15-42401642-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42401643dup , CM000677.2:g.42401643dup | GRCh38 |
| NC_000015.9:g.42693841dup , CM000677.1:g.42693841dup | GRCh37 |
| NC_000015.8:g.40481133dup | NCBI36 |
| NG_008660.1:g.58541dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1213dup | ENSP00000183936.4:p.Thr405AsnfsTer18 | |
| ENST00000357568.8:c.1357dup | ENSP00000350181.3:p.Thr453AsnfsTer18 | |
| ENST00000397163.8:c.1357dup MANE Select | ENSP00000380349.3:p.Thr453AsnfsTer18 | |
| ENST00000466369.5:n.1866dup | ||
| ENST00000483208.5:n.1588dup | ||
| ENST00000495723.1:n.1588dup | ||
| ENST00000549793.5:n.1588dup | ||
| ENST00000638141.2:n.1228dup | ||
| ENST00000673705.1:c.309+1991dup | ENSP00000501021.1:n.309+1991dup | |
| ENST00000318023.11:c.1213dup | ENSP00000326281.8:p.Thr405AsnfsTer18 | |
| ENST00000349748.7:c.1213dup | ENSP00000183936.4:p.Thr405AsnfsTer18 | |
| ENST00000357568.7:c.1357dup | ENSP00000350181.3:p.Thr453AsnfsTer18 | |
| ENST00000397163.7:c.1357dup | ENSP00000380349.3:p.Thr453AsnfsTer18 | |
| NM_000070.2:c.1357dup | NP_000061.1:p.Thr453AsnfsTer18 | |
| NM_024344.1:c.1357dup | NP_077320.1:p.Thr453AsnfsTer18 | |
| NM_173087.1:c.1213dup | NP_775110.1:p.Thr405AsnfsTer18 | |
| NM_000070.3:c.1357dup MANE Select | NP_000061.1:p.Thr453AsnfsTer18 | |
| NM_024344.2:c.1357dup | NP_077320.1:p.Thr453AsnfsTer18 | |
| NM_173087.2:c.1213dup | NP_775110.1:p.Thr405AsnfsTer18 |