Linked Data
ClinVar Variation Id:
198001
dbSNP Id:
rs141133453
ExAC:
14:102502958 C / T
gnomAD v2:
14-102502958-C-T
gnomAD v3:
14-102036621-C-T
gnomAD v4:
14-102036621-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102036621C>T , CM000676.2:g.102036621C>T | GRCh38 |
| NC_000014.8:g.102502958C>T , CM000676.1:g.102502958C>T | GRCh37 |
| NC_000014.7:g.101572711C>T | NCBI36 |
| NG_008777.1:g.77094C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684561.1:c.*2346C>T | ENSP00000506816.1:n.*2346C>T | |
| ENST00000360184.10:c.10887C>T MANE Select | ENSP00000348965.4:p.Phe3629= | |
| ENST00000557551.1:n.260G>A | ||
| ENST00000643437.1:n.841C>T | ||
| ENST00000643508.2:c.10887C>T | ENSP00000495528.2:p.Phe3629= | |
| ENST00000643722.1:n.3682C>T | ||
| ENST00000643829.1:n.716C>T | ||
| ENST00000644881.2:c.10887C>T | ENSP00000495022.2:p.Phe3629= | |
| ENST00000645039.2:c.10887C>T | ENSP00000495220.2:p.Phe3629= | |
| ENST00000645149.2:c.10887C>T | ENSP00000495944.2:p.Phe3629= | |
| ENST00000645697.1:n.1550C>T | ||
| ENST00000647204.2:n.128C>T | ||
| ENST00000647307.1:n.3630C>T | ||
| ENST00000647366.1:n.4441C>T | ||
| ENST00000679486.1:c.10887C>T | ENSP00000506688.1:p.Phe3629= | |
| ENST00000679629.1:c.10887C>T | ENSP00000505589.1:p.Phe3629= | |
| ENST00000679720.1:c.10887C>T | ENSP00000505938.1:p.Phe3629= | |
| ENST00000679910.1:c.*1969C>T | ENSP00000506521.1:n.*1969C>T | |
| ENST00000680120.1:c.10887C>T | ENSP00000504863.1:p.Phe3629= | |
| ENST00000680137.1:c.10887C>T | ENSP00000505294.1:p.Phe3629= | |
| ENST00000680200.1:c.*146C>T | ENSP00000506166.1:n.*146C>T | |
| ENST00000680313.1:c.10887C>T | ENSP00000506208.1:p.Phe3629= | |
| ENST00000680423.1:c.*2618C>T | ENSP00000505483.1:n.*2618C>T | |
| ENST00000680715.1:c.10887C>T | ENSP00000505332.1:p.Phe3629= | |
| ENST00000680874.1:c.*115C>T | ENSP00000504911.1:n.*115C>T | |
| ENST00000681010.1:c.10887C>T | ENSP00000505201.1:p.Phe3629= | |
| ENST00000681066.1:c.10887C>T | ENSP00000506344.1:p.Phe3629= | |
| ENST00000681123.1:c.10887C>T | ENSP00000506124.1:p.Phe3629= | |
| ENST00000681283.1:c.10887C>T | ENSP00000505667.1:p.Phe3629= | |
| ENST00000681536.1:c.*4086C>T | ENSP00000505821.1:n.*4086C>T | |
| ENST00000681574.1:c.10887C>T | ENSP00000505523.1:p.Phe3629= | |
| ENST00000681822.1:c.10887C>T | ENSP00000505744.1:p.Phe3629= | |
| ENST00000360184.8:c.10887C>T | ENSP00000348965.4:p.Phe3629= | |
| ENST00000553423.1:c.313C>T | ||
| ENST00000556791.1:n.811C>T | ||
| NM_001376.4:c.10887C>T | NP_001367.2:p.Phe3629= | |
| XR_001750903.1:n.236G>A | ||
| NM_001376.5:c.10887C>T MANE Select | NP_001367.2:p.Phe3629= |