Linked Data
ClinVar Variation Id:
214069
ClinVar RCV Id:
RCV000198428
dbSNP Id:
rs863223892
gnomAD v2:
7-141341172-C-T
gnomAD v4:
7-141641372-C-T
COSMIC:
COSM1086288
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141641372C>T , CM000669.2:g.141641372C>T | GRCh38 |
| NC_000007.13:g.141341172C>T , CM000669.1:g.141341172C>T | GRCh37 |
| NC_000007.12:g.140987641C>T | NCBI36 |
| NG_032079.1:g.95095C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647568.1:c.*814C>T | ENSP00000497039.1:n.*814C>T | |
| ENST00000648068.1:c.851C>T | ENSP00000498112.1:p.Ala284Val | |
| ENST00000648395.1:c.575C>T | ENSP00000497666.1:p.Ala192Val | |
| ENST00000648489.1:n.882C>T | ||
| ENST00000649014.1:c.*126C>T | ENSP00000497984.1:n.*126C>T | |
| ENST00000649286.2:c.851C>T MANE Select | ENSP00000497280.1:p.Ala284Val | |
| ENST00000649365.1:c.*859C>T | ENSP00000496835.1:n.*859C>T | |
| ENST00000649790.1:c.*287C>T | ENSP00000498193.1:n.*287C>T | |
| ENST00000649914.1:c.839C>T | ENSP00000497848.1:p.Ala280Val | |
| ENST00000650006.1:c.851C>T | ENSP00000497457.1:p.Ala284Val | |
| ENST00000650365.1:c.*736C>T | ENSP00000497358.1:n.*736C>T | |
| ENST00000650547.1:c.851C>T | ENSP00000496789.1:p.Ala284Val | |
| ENST00000355413.8:c.851C>T | ENSP00000347581.4:p.Ala284Val | |
| ENST00000473247.5:c.767C>T | ENSP00000420776.1:p.Ala256Val | |
| ENST00000494688.1:c.718-439C>T | ENSP00000418101.1:n.718-439C>T | |
| ENST00000629555.2:c.718-439C>T | ENSP00000487274.1:n.718-439C>T | |
| NM_018238.3:c.851C>T | NP_060708.1:p.Ala284Val | |
| XM_005250023.3:c.851C>T | XP_005250080.1:p.Ala284Val | |
| XM_011516397.1:c.851C>T | XP_011514699.1:p.Ala284Val | |
| NM_001364948.1:c.851C>T | NP_001351877.1:p.Ala284Val | |
| NM_018238.4:c.851C>T MANE Select | NP_060708.1:p.Ala284Val | |
| XM_011516397.3:c.851C>T | XP_011514699.1:p.Ala284Val | |
| XM_024446835.1:c.851C>T | XP_024302603.1:p.Ala284Val | |
| NM_001364948.2:c.851C>T | NP_001351877.1:p.Ala284Val | |
| NM_001364948.3:c.851C>T | NP_001351877.1:p.Ala284Val |