Linked Data
ClinVar Variation Id:
1043781
dbSNP Id:
rs769427505
ExAC:
2:48033354 G / A
gnomAD v2:
2-48033354-G-A
gnomAD v4:
2-47806215-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806215G>A , CM000664.2:g.47806215G>A | GRCh38 |
| NC_000002.11:g.48033354G>A , CM000664.1:g.48033354G>A | GRCh37 |
| NC_000002.10:g.47886858G>A | NCBI36 |
| NG_007111.1:g.28069G>A , LRG_219:g.28069G>A | |
| NG_008397.1:g.104461C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3361G>A (MSH6) | ENSP00000406248.2:p.Ala1121Thr | |
| ENST00000420813.6:c.3361G>A (MSH6) | ENSP00000390382.2:p.Ala1121Thr | |
| ENST00000455383.6:c.3361G>A (MSH6) | ENSP00000397484.2:p.Ala1121Thr | |
| ENST00000700004.2:c.3274G>A (MSH6) | ENSP00000514752.2:p.Ala1092Thr | |
| ENST00000699999.1:n.4332G>A (MSH6) | ||
| ENST00000700000.1:c.2092G>A (MSH6) | ENSP00000514749.1:p.Ala698Thr | |
| ENST00000700002.1:c.3664G>A (MSH6) | ENSP00000514750.1:p.Ala1222Thr | |
| ENST00000700003.1:c.1113G>A (MSH6) | ENSP00000514751.1:n.1113G>A | |
| ENST00000700004.1:c.2431G>A (MSH6) | ENSP00000514752.1:p.Ala811Thr | |
| ENST00000700005.1:n.2509G>A (MSH6) | ||
| ENST00000700006.1:n.4816G>A (MSH6) | ||
| ENST00000700007.1:n.2253G>A (MSH6) | ||
| ENST00000700008.1:n.1827G>A (MSH6) | ||
| ENST00000700009.1:n.2322G>A (MSH6) | ||
| ENST00000700010.1:n.1067G>A (MSH6) | ||
| ENST00000700011.1:n.2952G>A (MSH6) | ||
| ENST00000682451.1:n.4533C>T (FBXO11) | ||
| ENST00000684712.1:n.4795C>T (FBXO11) | ||
| ENST00000234420.11:c.3658G>A (MSH6) MANE Select | ENSP00000234420.5:p.Ala1220Thr | |
| ENST00000540021.6:c.3268G>A (MSH6) | ENSP00000446475.1:p.Ala1090Thr | |
| ENST00000652107.1:c.3361G>A (MSH6) | ENSP00000498629.1:p.Ala1121Thr | |
| ENST00000673637.1:c.3361G>A (MSH6) | ENSP00000501310.1:p.Ala1121Thr | |
| ENST00000234420.9:c.3658G>A (MSH6) | ENSP00000234420.4:p.Ala1220Thr | |
| ENST00000405808.5:c.169+1980C>T (FBXO11) | ENSP00000385127.1:n.169+1980C>T | |
| ENST00000434234.5:c.*124+1779C>T (FBXO11) | ENSP00000402692.1:n.*124+1779C>T | |
| ENST00000445503.5:c.*3005G>A (MSH6) | ENSP00000405294.1:n.*3005G>A | |
| ENST00000538136.1:c.2752G>A (MSH6) | ENSP00000438580.1:p.Ala918Thr | |
| ENST00000540021.5:c.3268G>A (MSH6) | ENSP00000446475.1:p.Ala1090Thr | |
| ENST00000614496.4:c.2752G>A (MSH6) | ENSP00000477844.1:p.Ala918Thr | |
| ENST00000622629.4:c.562G>A (MSH6) | ENSP00000482078.1:p.Ala188Thr | |
| NM_000179.2:c.3658G>A , LRG_219t1:c.3658G>A (MSH6) | NP_000170.1:p.Ala1220Thr | |
| NM_001281492.1:c.3268G>A (MSH6) | NP_001268421.1:p.Ala1090Thr | |
| NM_001281493.1:c.2752G>A (MSH6) | NP_001268422.1:p.Ala918Thr | |
| NM_001281494.1:c.2752G>A (MSH6) | NP_001268423.1:p.Ala918Thr | |
| XM_005264271.1:c.3361G>A (MSH6) | XP_005264328.1:p.Ala1121Thr | |
| XM_011532798.1:c.3475G>A (MSH6) | XP_011531100.1:p.Ala1159Thr | |
| XM_011532799.1:c.3361G>A (MSH6) | XP_011531101.1:p.Ala1121Thr | |
| XM_011532800.1:c.3361G>A (MSH6) | XP_011531102.1:p.Ala1121Thr | |
| XM_024452819.1:c.3658G>A (MSH6) | XP_024308587.1:p.Ala1220Thr | |
| XM_024452820.1:c.3475G>A (MSH6) | XP_024308588.1:p.Ala1159Thr | |
| XM_024452821.1:c.3361G>A (MSH6) | XP_024308589.1:p.Ala1121Thr | |
| XM_024452822.1:c.2752G>A (MSH6) | XP_024308590.1:p.Ala918Thr | |
| NM_000179.3:c.3658G>A (MSH6) MANE Select | NP_000170.1:p.Ala1220Thr | |
| NM_001281492.2:c.3268G>A (MSH6) | NP_001268421.1:p.Ala1090Thr | |
| NM_001281493.2:c.2752G>A (MSH6) | NP_001268422.1:p.Ala918Thr | |
| NM_001281494.2:c.2752G>A (MSH6) | NP_001268423.1:p.Ala918Thr |