Linked Data
ClinVar Variation Id:
188188
ClinVar RCV Id:
RCV000168100
RCV000213342
RCV000663216
RCV001800508
RCV003462256
RCV003987391
RCV003995607
dbSNP Id:
rs786204130
gnomAD v2:
2-48033921-A-C
gnomAD v3:
2-47806782-A-C
gnomAD v4:
2-47806782-A-C
PubMed:
PMID:23523604
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806782A>C , CM000664.2:g.47806782A>C | GRCh38 |
| NC_000002.11:g.48033921A>C , CM000664.1:g.48033921A>C | GRCh37 |
| NC_000002.10:g.47887425A>C | NCBI36 |
| NG_007111.1:g.28636A>C , LRG_219:g.28636A>C | |
| NG_008397.1:g.103894T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3708A>C (MSH6) | ENSP00000406248.2:p.Glu1236Asp | |
| ENST00000420813.6:c.3708A>C (MSH6) | ENSP00000390382.2:p.Glu1236Asp | |
| ENST00000455383.6:c.3708A>C (MSH6) | ENSP00000397484.2:p.Glu1236Asp | |
| ENST00000700004.2:c.3621A>C (MSH6) | ENSP00000514752.2:p.Glu1207Asp | |
| ENST00000699999.1:n.4679A>C (MSH6) | ||
| ENST00000700000.1:c.2439A>C (MSH6) | ENSP00000514749.1:p.Glu813Asp | |
| ENST00000700002.1:c.4011A>C (MSH6) | ENSP00000514750.1:p.Glu1337Asp | |
| ENST00000700003.1:c.1460A>C (MSH6) | ENSP00000514751.1:n.1460A>C | |
| ENST00000700004.1:c.2778A>C (MSH6) | ENSP00000514752.1:p.Glu926Asp | |
| ENST00000700005.1:n.2983A>C (MSH6) | ||
| ENST00000700007.1:n.2600A>C (MSH6) | ||
| ENST00000700008.1:n.2267A>C (MSH6) | ||
| ENST00000700009.1:n.2669A>C (MSH6) | ||
| ENST00000700010.1:n.1414A>C (MSH6) | ||
| ENST00000700011.1:n.3299A>C (MSH6) | ||
| ENST00000682451.1:n.3966T>G (FBXO11) | ||
| ENST00000684712.1:n.4228T>G (FBXO11) | ||
| ENST00000234420.11:c.4005A>C (MSH6) MANE Select | ENSP00000234420.5:p.Glu1335Asp | |
| ENST00000540021.6:c.3615A>C (MSH6) | ENSP00000446475.1:p.Glu1205Asp | |
| ENST00000652107.1:c.3708A>C (MSH6) | ENSP00000498629.1:p.Glu1236Asp | |
| ENST00000673637.1:c.3708A>C (MSH6) | ENSP00000501310.1:p.Glu1236Asp | |
| ENST00000234420.9:c.4005A>C (MSH6) | ENSP00000234420.4:p.Glu1335Asp | |
| ENST00000405808.5:c.169+1413T>G (FBXO11) | ENSP00000385127.1:n.169+1413T>G | |
| ENST00000434234.5:c.*124+1212T>G (FBXO11) | ENSP00000402692.1:n.*124+1212T>G | |
| ENST00000445503.5:c.*3352A>C (MSH6) | ENSP00000405294.1:n.*3352A>C | |
| ENST00000465204.5:n.3128T>G (FBXO11) | ||
| ENST00000538136.1:c.3099A>C (MSH6) | ENSP00000438580.1:p.Glu1033Asp | |
| ENST00000540021.5:c.3615A>C (MSH6) | ENSP00000446475.1:p.Glu1205Asp | |
| ENST00000614496.4:c.3099A>C (MSH6) | ENSP00000477844.1:p.Glu1033Asp | |
| ENST00000622629.4:c.906A>C (MSH6) | ENSP00000482078.1:p.Glu302Asp | |
| NM_000179.2:c.4005A>C , LRG_219t1:c.4005A>C (MSH6) | NP_000170.1:p.Glu1335Asp | |
| NM_001281492.1:c.3615A>C (MSH6) | NP_001268421.1:p.Glu1205Asp | |
| NM_001281493.1:c.3099A>C (MSH6) | NP_001268422.1:p.Glu1033Asp | |
| NM_001281494.1:c.3099A>C (MSH6) | NP_001268423.1:p.Glu1033Asp | |
| XM_005264271.1:c.3708A>C (MSH6) | XP_005264328.1:p.Glu1236Asp | |
| XM_011532798.1:c.3822A>C (MSH6) | XP_011531100.1:p.Glu1274Asp | |
| XM_011532799.1:c.3708A>C (MSH6) | XP_011531101.1:p.Glu1236Asp | |
| XM_011532800.1:c.3708A>C (MSH6) | XP_011531102.1:p.Glu1236Asp | |
| XM_024452819.1:c.4098A>C (MSH6) | XP_024308587.1:p.Glu1366Asp | |
| XM_024452820.1:c.3915A>C (MSH6) | XP_024308588.1:p.Glu1305Asp | |
| XM_024452821.1:c.3801A>C (MSH6) | XP_024308589.1:p.Glu1267Asp | |
| XM_024452822.1:c.3192A>C (MSH6) | XP_024308590.1:p.Glu1064Asp | |
| NM_000179.3:c.4005A>C (MSH6) MANE Select | NP_000170.1:p.Glu1335Asp | |
| NM_001281492.2:c.3615A>C (MSH6) | NP_001268421.1:p.Glu1205Asp | |
| NM_001281493.2:c.3099A>C (MSH6) | NP_001268422.1:p.Glu1033Asp | |
| NM_001281494.2:c.3099A>C (MSH6) | NP_001268423.1:p.Glu1033Asp |