Linked Data
ClinVar Variation Id:
305954
dbSNP Id:
rs567600444
ExAC:
11:71146758 G / A
gnomAD v2:
11-71146758-G-A
gnomAD v3:
11-71435712-G-A
gnomAD v4:
11-71435712-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435712G>A , CM000673.2:g.71435712G>A | GRCh38 |
| NC_000011.9:g.71146758G>A , CM000673.1:g.71146758G>A | GRCh37 |
| NC_000011.8:g.70824406G>A | NCBI36 |
| NG_012655.2:g.17720C>T , LRG_340:g.17720C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1091C>T | ENSP00000435707.3:p.Thr364Met | |
| ENST00000526780.6:c.1091C>T | ENSP00000435668.2:p.Thr364Met | |
| ENST00000527316.6:c.917C>T | ENSP00000435047.2:p.Thr306Met | |
| ENST00000682708.1:c.1142C>T | ENSP00000506866.1:p.Thr381Met | |
| ENST00000683287.1:c.1127C>T | ENSP00000507607.1:p.Thr376Met | |
| ENST00000683714.1:c.1099C>T | ENSP00000508207.1:p.Arg367Trp | |
| ENST00000684396.1:n.1131C>T | ||
| ENST00000685320.1:c.506C>T | ENSP00000509319.1:p.Thr169Met | |
| ENST00000690257.1:c.995C>T | ENSP00000510750.1:p.Thr332Met | |
| ENST00000355527.8:c.1091C>T MANE Select | ENSP00000347717.4:p.Thr364Met | |
| ENST00000355527.7:c.1091C>T | ENSP00000347717.3:p.Thr364Met | |
| ENST00000407721.6:c.1091C>T | ENSP00000384739.2:p.Thr364Met | |
| ENST00000525137.1:c.592C>T | ENSP00000435956.1:p.Arg198Trp | |
| ENST00000533800.5:c.341C>T | ENSP00000435011.1:p.Thr114Met | |
| ENST00000534795.5:c.319+2100C>T | ||
| NM_001163817.1:c.1091C>T | NP_001157289.1:p.Thr364Met | |
| NM_001360.2:c.1091C>T , LRG_340t1:c.1091C>T | NP_001351.2:p.Thr364Met | |
| XM_011544777.1:c.1225C>T | XP_011543079.1:p.Arg409Trp | |
| XM_011544777.2:c.1225C>T | XP_011543079.1:p.Arg409Trp | |
| NM_001163817.2:c.1091C>T | NP_001157289.1:p.Thr364Met | |
| NM_001360.3:c.1091C>T MANE Select | NP_001351.2:p.Thr364Met |