Linked Data
ClinVar Variation Id:
594763
dbSNP Id:
rs777517985
ExAC:
11:71146694 G / A
gnomAD v2:
11-71146694-G-A
gnomAD v3:
11-71435648-G-A
gnomAD v4:
11-71435648-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435648G>A , CM000673.2:g.71435648G>A | GRCh38 |
| NC_000011.9:g.71146694G>A , CM000673.1:g.71146694G>A | GRCh37 |
| NC_000011.8:g.70824342G>A | NCBI36 |
| NG_012655.2:g.17784C>T , LRG_340:g.17784C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1155C>T | ENSP00000435707.3:p.Ala385= | |
| ENST00000526780.6:c.1155C>T | ENSP00000435668.2:p.Ala385= | |
| ENST00000527316.6:c.981C>T | ENSP00000435047.2:p.Ala327= | |
| ENST00000682708.1:c.1206C>T | ENSP00000506866.1:p.Ala402= | |
| ENST00000683287.1:c.1191C>T | ENSP00000507607.1:p.Ala397= | |
| ENST00000683714.1:c.1163C>T | ENSP00000508207.1:p.Pro388Leu | |
| ENST00000684396.1:n.1195C>T | ||
| ENST00000685320.1:c.570C>T | ENSP00000509319.1:p.Ala190= | |
| ENST00000690257.1:c.1059C>T | ENSP00000510750.1:p.Ala353= | |
| ENST00000355527.8:c.1155C>T MANE Select | ENSP00000347717.4:p.Ala385= | |
| ENST00000355527.7:c.1155C>T | ENSP00000347717.3:p.Ala385= | |
| ENST00000407721.6:c.1155C>T | ENSP00000384739.2:p.Ala385= | |
| ENST00000525137.1:c.656C>T | ENSP00000435956.1:p.Pro219Leu | |
| ENST00000533800.5:c.405C>T | ENSP00000435011.1:p.Ala135= | |
| ENST00000534795.5:c.319+2164C>T | ||
| NM_001163817.1:c.1155C>T | NP_001157289.1:p.Ala385= | |
| NM_001360.2:c.1155C>T , LRG_340t1:c.1155C>T | NP_001351.2:p.Ala385= | |
| XM_011544777.1:c.1289C>T | XP_011543079.1:p.Pro430Leu | |
| XM_011544777.2:c.1289C>T | XP_011543079.1:p.Pro430Leu | |
| NM_001163817.2:c.1155C>T | NP_001157289.1:p.Ala385= | |
| NM_001360.3:c.1155C>T MANE Select | NP_001351.2:p.Ala385= |