Linked Data
ClinVar Variation Id:
284741
ClinVar RCV Id:
RCV000392552
dbSNP Id:
rs755252656
gnomAD v2:
14-31349663-C-T
gnomAD v3:
14-30880457-C-T
gnomAD v4:
14-30880457-C-T
COSMIC:
COSM1201740
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.30880457C>T , CM000676.2:g.30880457C>T | GRCh38 |
| NC_000014.8:g.31349663C>T , CM000676.1:g.31349663C>T | GRCh37 |
| NC_000014.7:g.30419414C>T | NCBI36 |
| NG_008211.2:g.10923C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216361.9:c.637C>T | ENSP00000216361.5:p.Arg213Ter | |
| ENST00000396618.9:c.442C>T MANE Select | ENSP00000379862.3:p.Arg148Ter | |
| ENST00000555117.2:c.442C>T | ENSP00000493569.1:p.Arg148Ter | |
| ENST00000643575.1:c.442C>T | ENSP00000494838.1:p.Arg148Ter | |
| ENST00000643697.1:n.687C>T | ||
| ENST00000644874.2:c.442C>T | ENSP00000496360.1:p.Arg148Ter | |
| ENST00000216361.8:c.442C>T | ENSP00000216361.4:p.Arg148Ter | |
| ENST00000396618.7:c.442C>T | ENSP00000379862.3:p.Arg148Ter | |
| ENST00000460581.6:c.106C>T | ENSP00000451713.1:p.Arg36Ter | |
| ENST00000475087.5:c.442C>T | ENSP00000451528.1:p.Arg148Ter | |
| ENST00000553772.5:c.*2C>T | ENSP00000452343.1:n.*2C>T | |
| ENST00000553833.5:n.596C>T | ||
| ENST00000555881.5:c.88C>T | ENSP00000452569.1:p.Arg30Ter | |
| ENST00000556908.5:c.394C>T | ENSP00000452541.1:p.Arg132Ter | |
| ENST00000557065.1:c.224C>T | ENSP00000451629.1:n.224C>T | |
| NM_001135058.1:c.442C>T | NP_001128530.1:p.Arg148Ter | |
| NM_004086.2:c.442C>T | NP_004077.1:p.Arg148Ter | |
| NR_038356.1:n.1618-3905G>A | ||
| XM_011536539.1:c.442C>T | XP_011534841.1:p.Arg148Ter | |
| NM_001347720.1:c.637C>T | NP_001334649.1:p.Arg213Ter | |
| XM_017021071.1:c.637C>T | XP_016876560.1:p.Arg213Ter | |
| XM_024449506.1:c.442C>T | XP_024305274.1:p.Arg148Ter | |
| NM_004086.3:c.442C>T MANE Select | NP_004077.1:p.Arg148Ter | |
| NM_001135058.2:c.442C>T | NP_001128530.1:p.Arg148Ter | |
| NM_001347720.2:c.637C>T | NP_001334649.1:p.Arg213Ter |