Linked Data
ClinVar Variation Id:
2811649
ClinVar RCV Id:
RCV003618404
MyVariant Identifiers:
chr11:g.71146493G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435447G>A , CM000673.2:g.71435447G>A | GRCh38 |
| NC_000011.9:g.71146493G>A , CM000673.1:g.71146493G>A | GRCh37 |
| NC_000011.8:g.70824141G>A | NCBI36 |
| NG_012655.2:g.17985C>T , LRG_340:g.17985C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1356C>T | ENSP00000435707.3:p.Ala452= | |
| ENST00000526780.6:c.1356C>T | ENSP00000435668.2:p.Ala452= | |
| ENST00000527316.6:c.1182C>T | ENSP00000435047.2:p.Ala394= | |
| ENST00000682708.1:c.1407C>T | ENSP00000506866.1:p.Ala469= | |
| ENST00000683287.1:c.1392C>T | ENSP00000507607.1:p.Ala464= | |
| ENST00000683714.1:c.*119C>T | ENSP00000508207.1:n.*119C>T | |
| ENST00000684396.1:n.1396C>T | ||
| ENST00000685320.1:c.771C>T | ENSP00000509319.1:p.Ala257= | |
| ENST00000690257.1:c.1260C>T | ENSP00000510750.1:p.Ala420= | |
| ENST00000355527.8:c.1356C>T MANE Select | ENSP00000347717.4:p.Ala452= | |
| ENST00000355527.7:c.1356C>T | ENSP00000347717.3:p.Ala452= | |
| ENST00000407721.6:c.1356C>T | ENSP00000384739.2:p.Ala452= | |
| ENST00000525137.1:c.857C>T | ENSP00000435956.1:n.857C>T | |
| ENST00000533800.5:c.606C>T | ENSP00000435011.1:p.Ala202= | |
| ENST00000534795.5:c.319+2365C>T | ||
| NM_001163817.1:c.1356C>T | NP_001157289.1:p.Ala452= | |
| NM_001360.2:c.1356C>T , LRG_340t1:c.1356C>T | NP_001351.2:p.Ala452= | |
| XM_011544777.1:c.*119C>T | XP_011543079.1:n.*119C>T | |
| XM_011544777.2:c.*119C>T | XP_011543079.1:n.*119C>T | |
| NM_001163817.2:c.1356C>T | NP_001157289.1:p.Ala452= | |
| NM_001360.3:c.1356C>T MANE Select | NP_001351.2:p.Ala452= |