Linked Data
ClinVar Variation Id:
233214
dbSNP Id:
rs267608122
gnomAD v4:
2-47806651-G-C
PubMed:
PMID:23588873
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806651G>C , CM000664.2:g.47806651G>C | GRCh38 |
| NC_000002.11:g.48033790G>C , CM000664.1:g.48033790G>C | GRCh37 |
| NC_000002.10:g.47887294G>C | NCBI36 |
| NG_007111.1:g.28505G>C , LRG_219:g.28505G>C | |
| NG_008397.1:g.104025C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3704G>C (MSH6) | ENSP00000406248.2:p.Arg1235Pro | |
| ENST00000420813.6:c.3704G>C (MSH6) | ENSP00000390382.2:p.Arg1235Pro | |
| ENST00000455383.6:c.3704G>C (MSH6) | ENSP00000397484.2:p.Arg1235Pro | |
| ENST00000700004.2:c.3617G>C (MSH6) | ENSP00000514752.2:p.Arg1206Pro | |
| ENST00000699999.1:n.4675G>C (MSH6) | ||
| ENST00000700000.1:c.2435G>C (MSH6) | ENSP00000514749.1:p.Arg812Pro | |
| ENST00000700002.1:c.4007G>C (MSH6) | ENSP00000514750.1:p.Arg1336Pro | |
| ENST00000700003.1:c.1456G>C (MSH6) | ENSP00000514751.1:n.1456G>C | |
| ENST00000700004.1:c.2774G>C (MSH6) | ENSP00000514752.1:p.Arg925Pro | |
| ENST00000700005.1:n.2852G>C (MSH6) | ||
| ENST00000700006.1:n.5159G>C (MSH6) | ||
| ENST00000700007.1:n.2596G>C (MSH6) | ||
| ENST00000700008.1:n.2263G>C (MSH6) | ||
| ENST00000700009.1:n.2665G>C (MSH6) | ||
| ENST00000700010.1:n.1410G>C (MSH6) | ||
| ENST00000700011.1:n.3295G>C (MSH6) | ||
| ENST00000682451.1:n.4097C>G (FBXO11) | ||
| ENST00000684712.1:n.4359C>G (FBXO11) | ||
| ENST00000234420.11:c.4001G>C (MSH6) MANE Select | ENSP00000234420.5:p.Arg1334Pro | |
| ENST00000540021.6:c.3611G>C (MSH6) | ENSP00000446475.1:p.Arg1204Pro | |
| ENST00000652107.1:c.3704G>C (MSH6) | ENSP00000498629.1:p.Arg1235Pro | |
| ENST00000673637.1:c.3704G>C (MSH6) | ENSP00000501310.1:p.Arg1235Pro | |
| ENST00000234420.9:c.4001G>C (MSH6) | ENSP00000234420.4:p.Arg1334Pro | |
| ENST00000405808.5:c.169+1544C>G (FBXO11) | ENSP00000385127.1:n.169+1544C>G | |
| ENST00000434234.5:c.*124+1343C>G (FBXO11) | ENSP00000402692.1:n.*124+1343C>G | |
| ENST00000445503.5:c.*3348G>C (MSH6) | ENSP00000405294.1:n.*3348G>C | |
| ENST00000538136.1:c.3095G>C (MSH6) | ENSP00000438580.1:p.Arg1032Pro | |
| ENST00000540021.5:c.3611G>C (MSH6) | ENSP00000446475.1:p.Arg1204Pro | |
| ENST00000614496.4:c.3095G>C (MSH6) | ENSP00000477844.1:p.Arg1032Pro | |
| ENST00000622629.4:c.902G>C (MSH6) | ENSP00000482078.1:p.Arg301Pro | |
| NM_000179.2:c.4001G>C , LRG_219t1:c.4001G>C (MSH6) | NP_000170.1:p.Arg1334Pro | |
| NM_001281492.1:c.3611G>C (MSH6) | NP_001268421.1:p.Arg1204Pro | |
| NM_001281493.1:c.3095G>C (MSH6) | NP_001268422.1:p.Arg1032Pro | |
| NM_001281494.1:c.3095G>C (MSH6) | NP_001268423.1:p.Arg1032Pro | |
| XM_005264271.1:c.3704G>C (MSH6) | XP_005264328.1:p.Arg1235Pro | |
| XM_011532798.1:c.3818G>C (MSH6) | XP_011531100.1:p.Arg1273Pro | |
| XM_011532799.1:c.3704G>C (MSH6) | XP_011531101.1:p.Arg1235Pro | |
| XM_011532800.1:c.3704G>C (MSH6) | XP_011531102.1:p.Arg1235Pro | |
| XM_024452819.1:c.4094G>C (MSH6) | XP_024308587.1:p.Arg1365Pro | |
| XM_024452820.1:c.3911G>C (MSH6) | XP_024308588.1:p.Arg1304Pro | |
| XM_024452821.1:c.3797G>C (MSH6) | XP_024308589.1:p.Arg1266Pro | |
| XM_024452822.1:c.3188G>C (MSH6) | XP_024308590.1:p.Arg1063Pro | |
| NM_000179.3:c.4001G>C (MSH6) MANE Select | NP_000170.1:p.Arg1334Pro | |
| NM_001281492.2:c.3611G>C (MSH6) | NP_001268421.1:p.Arg1204Pro | |
| NM_001281493.2:c.3095G>C (MSH6) | NP_001268422.1:p.Arg1032Pro | |
| NM_001281494.2:c.3095G>C (MSH6) | NP_001268423.1:p.Arg1032Pro |