Linked Data
ClinVar Variation Id:
410393
dbSNP Id:
rs575714670
gnomAD v2:
2-48033675-A-G
gnomAD v3:
2-47806536-A-G
gnomAD v4:
2-47806536-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806536A>G , CM000664.2:g.47806536A>G | GRCh38 |
| NC_000002.11:g.48033675A>G , CM000664.1:g.48033675A>G | GRCh37 |
| NC_000002.10:g.47887179A>G | NCBI36 |
| NG_007111.1:g.28390A>G , LRG_219:g.28390A>G | |
| NG_008397.1:g.104140T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3589A>G (MSH6) | ENSP00000406248.2:p.Lys1197Glu | |
| ENST00000420813.6:c.3589A>G (MSH6) | ENSP00000390382.2:p.Lys1197Glu | |
| ENST00000455383.6:c.3589A>G (MSH6) | ENSP00000397484.2:p.Lys1197Glu | |
| ENST00000700004.2:c.3502A>G (MSH6) | ENSP00000514752.2:p.Lys1168Glu | |
| ENST00000699999.1:n.4560A>G (MSH6) | ||
| ENST00000700000.1:c.2320A>G (MSH6) | ENSP00000514749.1:p.Lys774Glu | |
| ENST00000700002.1:c.3892A>G (MSH6) | ENSP00000514750.1:p.Lys1298Glu | |
| ENST00000700003.1:c.1341A>G (MSH6) | ENSP00000514751.1:n.1341A>G | |
| ENST00000700004.1:c.2659A>G (MSH6) | ENSP00000514752.1:p.Lys887Glu | |
| ENST00000700005.1:n.2737A>G (MSH6) | ||
| ENST00000700006.1:n.5044A>G (MSH6) | ||
| ENST00000700007.1:n.2481A>G (MSH6) | ||
| ENST00000700008.1:n.2148A>G (MSH6) | ||
| ENST00000700009.1:n.2550A>G (MSH6) | ||
| ENST00000700010.1:n.1295A>G (MSH6) | ||
| ENST00000700011.1:n.3180A>G (MSH6) | ||
| ENST00000682451.1:n.4212T>C (FBXO11) | ||
| ENST00000684712.1:n.4474T>C (FBXO11) | ||
| ENST00000234420.11:c.3886A>G (MSH6) MANE Select | ENSP00000234420.5:p.Lys1296Glu | |
| ENST00000540021.6:c.3496A>G (MSH6) | ENSP00000446475.1:p.Lys1166Glu | |
| ENST00000652107.1:c.3589A>G (MSH6) | ENSP00000498629.1:p.Lys1197Glu | |
| ENST00000673637.1:c.3589A>G (MSH6) | ENSP00000501310.1:p.Lys1197Glu | |
| ENST00000234420.9:c.3886A>G (MSH6) | ENSP00000234420.4:p.Lys1296Glu | |
| ENST00000405808.5:c.169+1659T>C (FBXO11) | ENSP00000385127.1:n.169+1659T>C | |
| ENST00000434234.5:c.*124+1458T>C (FBXO11) | ENSP00000402692.1:n.*124+1458T>C | |
| ENST00000445503.5:c.*3233A>G (MSH6) | ENSP00000405294.1:n.*3233A>G | |
| ENST00000538136.1:c.2980A>G (MSH6) | ENSP00000438580.1:p.Lys994Glu | |
| ENST00000540021.5:c.3496A>G (MSH6) | ENSP00000446475.1:p.Lys1166Glu | |
| ENST00000614496.4:c.2980A>G (MSH6) | ENSP00000477844.1:p.Lys994Glu | |
| ENST00000622629.4:c.787A>G (MSH6) | ENSP00000482078.1:p.Lys263Glu | |
| NM_000179.2:c.3886A>G , LRG_219t1:c.3886A>G (MSH6) | NP_000170.1:p.Lys1296Glu | |
| NM_001281492.1:c.3496A>G (MSH6) | NP_001268421.1:p.Lys1166Glu | |
| NM_001281493.1:c.2980A>G (MSH6) | NP_001268422.1:p.Lys994Glu | |
| NM_001281494.1:c.2980A>G (MSH6) | NP_001268423.1:p.Lys994Glu | |
| XM_005264271.1:c.3589A>G (MSH6) | XP_005264328.1:p.Lys1197Glu | |
| XM_011532798.1:c.3703A>G (MSH6) | XP_011531100.1:p.Lys1235Glu | |
| XM_011532799.1:c.3589A>G (MSH6) | XP_011531101.1:p.Lys1197Glu | |
| XM_011532800.1:c.3589A>G (MSH6) | XP_011531102.1:p.Lys1197Glu | |
| XM_024452819.1:c.3979A>G (MSH6) | XP_024308587.1:p.Lys1327Glu | |
| XM_024452820.1:c.3796A>G (MSH6) | XP_024308588.1:p.Lys1266Glu | |
| XM_024452821.1:c.3682A>G (MSH6) | XP_024308589.1:p.Lys1228Glu | |
| XM_024452822.1:c.3073A>G (MSH6) | XP_024308590.1:p.Lys1025Glu | |
| NM_000179.3:c.3886A>G (MSH6) MANE Select | NP_000170.1:p.Lys1296Glu | |
| NM_001281492.2:c.3496A>G (MSH6) | NP_001268421.1:p.Lys1166Glu | |
| NM_001281493.2:c.2980A>G (MSH6) | NP_001268422.1:p.Lys994Glu | |
| NM_001281494.2:c.2980A>G (MSH6) | NP_001268423.1:p.Lys994Glu |