Linked Data
ClinVar Variation Id:
135841
ClinVar RCV Id:
RCV000122963
RCV000128933
RCV000411062
RCV000587527
RCV001255217
RCV001354177
RCV003149837
dbSNP Id:
rs63750998
ExAC:
2:48030645 C / G
gnomAD v2:
2-48030645-C-G
gnomAD v3:
2-47803506-C-G
gnomAD v4:
2-47803506-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47803506C>G , CM000664.2:g.47803506C>G | GRCh38 |
| NC_000002.11:g.48030645C>G , CM000664.1:g.48030645C>G | GRCh37 |
| NC_000002.10:g.47884149C>G | NCBI36 |
| NG_007111.1:g.25360C>G , LRG_219:g.25360C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.2962C>G (MSH6) | ENSP00000406248.2:p.Pro988Ala | |
| ENST00000420813.6:c.2962C>G (MSH6) | ENSP00000390382.2:p.Pro988Ala | |
| ENST00000455383.6:c.2962C>G (MSH6) | ENSP00000397484.2:p.Pro988Ala | |
| ENST00000700004.2:c.3173-2112C>G (MSH6) | ENSP00000514752.2:n.3173-2112C>G | |
| ENST00000699999.1:n.3343C>G (MSH6) | ||
| ENST00000700000.1:c.1693C>G (MSH6) | ENSP00000514749.1:p.Pro565Ala | |
| ENST00000700002.1:c.3265C>G (MSH6) | ENSP00000514750.1:p.Pro1089Ala | |
| ENST00000700003.1:c.714C>G (MSH6) | ENSP00000514751.1:n.714C>G | |
| ENST00000700004.1:c.2330-2112C>G (MSH6) | ENSP00000514752.1:n.2330-2112C>G | |
| ENST00000700005.1:n.2110C>G (MSH6) | ||
| ENST00000700006.1:n.2107C>G (MSH6) | ||
| ENST00000700007.1:n.1264C>G (MSH6) | ||
| ENST00000700008.1:n.838C>G (MSH6) | ||
| ENST00000700009.1:n.837C>G (MSH6) | ||
| ENST00000700010.1:n.668C>G (MSH6) | ||
| ENST00000700011.1:n.739C>G (MSH6) | ||
| ENST00000234420.11:c.3259C>G (MSH6) MANE Select | ENSP00000234420.5:p.Pro1087Ala | |
| ENST00000540021.6:c.2869C>G (MSH6) | ENSP00000446475.1:p.Pro957Ala | |
| ENST00000652107.1:c.2962C>G (MSH6) | ENSP00000498629.1:p.Pro988Ala | |
| ENST00000673637.1:c.2962C>G (MSH6) | ENSP00000501310.1:p.Pro988Ala | |
| ENST00000234420.9:c.3259C>G (MSH6) | ENSP00000234420.4:p.Pro1087Ala | |
| ENST00000405808.5:c.169+4689G>C (FBXO11) | ENSP00000385127.1:n.169+4689G>C | |
| ENST00000434234.5:c.*124+4488G>C (FBXO11) | ENSP00000402692.1:n.*124+4488G>C | |
| ENST00000445503.5:c.*2606C>G (MSH6) | ENSP00000405294.1:n.*2606C>G | |
| ENST00000538136.1:c.2353C>G (MSH6) | ENSP00000438580.1:p.Pro785Ala | |
| ENST00000540021.5:c.2869C>G (MSH6) | ENSP00000446475.1:p.Pro957Ala | |
| ENST00000614496.4:c.2353C>G (MSH6) | ENSP00000477844.1:p.Pro785Ala | |
| ENST00000622629.4:c.163C>G (MSH6) | ENSP00000482078.1:p.Pro55Ala | |
| NM_000179.2:c.3259C>G , LRG_219t1:c.3259C>G (MSH6) | NP_000170.1:p.Pro1087Ala | |
| NM_001281492.1:c.2869C>G (MSH6) | NP_001268421.1:p.Pro957Ala | |
| NM_001281493.1:c.2353C>G (MSH6) | NP_001268422.1:p.Pro785Ala | |
| NM_001281494.1:c.2353C>G (MSH6) | NP_001268423.1:p.Pro785Ala | |
| XM_005264271.1:c.2962C>G (MSH6) | XP_005264328.1:p.Pro988Ala | |
| XM_011532798.1:c.3076C>G (MSH6) | XP_011531100.1:p.Pro1026Ala | |
| XM_011532799.1:c.2962C>G (MSH6) | XP_011531101.1:p.Pro988Ala | |
| XM_011532800.1:c.2962C>G (MSH6) | XP_011531102.1:p.Pro988Ala | |
| XM_024452819.1:c.3259C>G (MSH6) | XP_024308587.1:p.Pro1087Ala | |
| XM_024452820.1:c.3076C>G (MSH6) | XP_024308588.1:p.Pro1026Ala | |
| XM_024452821.1:c.2962C>G (MSH6) | XP_024308589.1:p.Pro988Ala | |
| XM_024452822.1:c.2353C>G (MSH6) | XP_024308590.1:p.Pro785Ala | |
| NM_000179.3:c.3259C>G (MSH6) MANE Select | NP_000170.1:p.Pro1087Ala | |
| NM_001281492.2:c.2869C>G (MSH6) | NP_001268421.1:p.Pro957Ala | |
| NM_001281493.2:c.2353C>G (MSH6) | NP_001268422.1:p.Pro785Ala | |
| NM_001281494.2:c.2353C>G (MSH6) | NP_001268423.1:p.Pro785Ala |