Linked Data
ClinVar Variation Id:
2576791
ClinVar RCV Id:
RCV003323096
dbSNP Id:
rs957258787
gnomAD v4:
10-121515179-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121515179A>C , CM000672.2:g.121515179A>C | GRCh38 |
| NC_000010.10:g.123274693A>C , CM000672.1:g.123274693A>C | GRCh37 |
| NC_000010.9:g.123264683A>C | NCBI36 |
| NG_012449.1:g.88280T>G | |
| NG_012449.2:g.88280T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000457416.7:c.1228T>G MANE Plus Clinical | ENSP00000410294.2:p.Phe410Val | |
| ENST00000351936.11:c.1225T>G | ENSP00000309878.10:p.Phe409Val | |
| ENST00000638709.2:c.55T>G | ENSP00000491912.2:p.Phe19Val | |
| ENST00000682296.1:n.573T>G | ||
| ENST00000682550.1:c.880T>G | ENSP00000507633.1:p.Phe294Val | |
| ENST00000682772.1:c.55T>G | ENSP00000506848.1:p.Phe19Val | |
| ENST00000683211.1:c.1225T>G | ENSP00000508257.1:p.Phe409Val | |
| ENST00000683250.1:c.404-11238T>G | ENSP00000506847.1:n.404-11238T>G | |
| ENST00000683418.1:n.3572T>G | ||
| ENST00000684153.1:c.880T>G | ENSP00000506937.1:p.Phe294Val | |
| ENST00000358487.10:c.1225T>G MANE Select | ENSP00000351276.6:p.Phe409Val | |
| ENST00000336553.10:c.958T>G | ENSP00000337665.6:p.Phe320Val | |
| ENST00000346997.6:c.1225T>G | ENSP00000263451.5:p.Phe409Val | |
| ENST00000351936.10:c.1231T>G | ENSP00000309878.9:p.Phe411Val | |
| ENST00000356226.8:c.880T>G | ENSP00000348559.4:p.Phe294Val | |
| ENST00000357555.9:c.958T>G | ENSP00000350166.5:p.Phe320Val | |
| ENST00000358487.9:c.1225T>G | ENSP00000351276.5:p.Phe409Val | |
| ENST00000360144.7:c.961T>G | ENSP00000353262.3:p.Phe321Val | |
| ENST00000369056.5:c.1228T>G | ENSP00000358052.1:p.Phe410Val | |
| ENST00000369058.7:c.1228T>G | ENSP00000358054.3:p.Phe410Val | |
| ENST00000369059.5:c.883T>G | ENSP00000358055.1:p.Phe295Val | |
| ENST00000369060.8:c.939+4800T>G | ENSP00000358056.4:n.939+4800T>G | |
| ENST00000369061.8:c.889T>G | ENSP00000358057.4:p.Phe297Val | |
| ENST00000429361.5:c.1T>G | ENSP00000404219.1:p.Phe1Val | |
| ENST00000457416.6:c.1228T>G | ENSP00000410294.2:p.Phe410Val | |
| ENST00000478859.5:c.541T>G | ENSP00000474011.1:p.Phe181Val | |
| ENST00000604236.5:c.*272T>G | ENSP00000474109.1:n.*272T>G | |
| ENST00000613048.4:c.958T>G | ENSP00000484154.1:p.Phe320Val | |
| NM_000141.4:c.1225T>G | NP_000132.3:p.Phe409Val | |
| NM_001144913.1:c.1228T>G | NP_001138385.1:p.Phe410Val | |
| NM_001144914.1:c.889T>G | NP_001138386.1:p.Phe297Val | |
| NM_001144915.1:c.958T>G | NP_001138387.1:p.Phe320Val | |
| NM_001144916.1:c.880T>G | NP_001138388.1:p.Phe294Val | |
| NM_001144917.1:c.939+4800T>G | NP_001138389.1:n.939+4800T>G | |
| NM_001144918.1:c.880T>G | NP_001138390.1:p.Phe294Val | |
| NM_001144919.1:c.961T>G | NP_001138391.1:p.Phe321Val | |
| NM_022970.3:c.1228T>G | NP_075259.4:p.Phe410Val | |
| NM_023029.2:c.958T>G | NP_075418.1:p.Phe320Val | |
| NR_073009.1:n.1675T>G | ||
| XM_006717708.2:c.1285T>G | XP_006717771.1:p.Phe429Val | |
| XM_006717709.2:c.1282T>G | XP_006717772.1:p.Phe428Val | |
| XM_006717710.2:c.1285T>G | XP_006717773.1:p.Phe429Val | |
| XM_006717711.2:c.1018T>G | XP_006717774.1:p.Phe340Val | |
| XM_006717712.2:c.940T>G | XP_006717775.1:p.Phe314Val | |
| XM_006717713.2:c.1282T>G | XP_006717776.1:p.Phe428Val | |
| XM_011539510.1:c.541T>G | XP_011537812.1:p.Phe181Val | |
| NM_001320654.1:c.541T>G | NP_001307583.1:p.Phe181Val | |
| NM_001320658.1:c.1225T>G | NP_001307587.1:p.Phe409Val | |
| XM_006717708.3:c.1285T>G | XP_006717771.1:p.Phe429Val | |
| XM_006717710.4:c.1285T>G | XP_006717773.1:p.Phe429Val | |
| XM_017015920.2:c.1285T>G | XP_016871409.1:p.Phe429Val | |
| XM_017015921.2:c.1282T>G | XP_016871410.1:p.Phe428Val | |
| XM_017015924.2:c.937T>G | XP_016871413.1:p.Phe313Val | |
| XM_017015925.2:c.937T>G | XP_016871414.1:p.Phe313Val | |
| XM_024447887.1:c.1015T>G | XP_024303655.1:p.Phe339Val | |
| XM_024447888.1:c.1018T>G | XP_024303656.1:p.Phe340Val | |
| XM_024447889.1:c.1015T>G | XP_024303657.1:p.Phe339Val | |
| XM_024447890.1:c.1018T>G | XP_024303658.1:p.Phe340Val | |
| XM_024447891.1:c.940T>G | XP_024303659.1:p.Phe314Val | |
| XM_024447892.1:c.55T>G | XP_024303660.1:p.Phe19Val | |
| NM_000141.5:c.1225T>G MANE Select | NP_000132.3:p.Phe409Val | |
| NM_001144917.2:c.939+4800T>G | NP_001138389.1:n.939+4800T>G | |
| NM_001144918.2:c.880T>G | NP_001138390.1:p.Phe294Val | |
| NM_001144919.2:c.961T>G | NP_001138391.1:p.Phe321Val | |
| NM_001320658.2:c.1225T>G | NP_001307587.1:p.Phe409Val | |
| NR_073009.2:n.1661T>G | ||
| NM_001144915.2:c.958T>G | NP_001138387.1:p.Phe320Val | |
| NM_001144916.2:c.880T>G | NP_001138388.1:p.Phe294Val | |
| NM_001320654.2:c.541T>G | NP_001307583.1:p.Phe181Val |