Linked Data
ClinVar Variation Id:
89490
ClinVar RCV Id:
RCV000074958
RCV000148646
RCV000115425
RCV000202255
RCV000410058
RCV000590664
RCV001082577
RCV001355442
RCV004528273
dbSNP Id:
rs41295278
ExAC:
2:48033750 A / G
gnomAD v2:
2-48033750-A-G
gnomAD v3:
2-47806611-A-G
gnomAD v4:
2-47806611-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47806611A>G , CM000664.2:g.47806611A>G | GRCh38 |
| NC_000002.11:g.48033750A>G , CM000664.1:g.48033750A>G | GRCh37 |
| NC_000002.10:g.47887254A>G | NCBI36 |
| NG_007111.1:g.28465A>G , LRG_219:g.28465A>G | |
| NG_008397.1:g.104065T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3664A>G (MSH6) | ENSP00000406248.2:p.Arg1222Gly | |
| ENST00000420813.6:c.3664A>G (MSH6) | ENSP00000390382.2:p.Arg1222Gly | |
| ENST00000455383.6:c.3664A>G (MSH6) | ENSP00000397484.2:p.Arg1222Gly | |
| ENST00000700004.2:c.3577A>G (MSH6) | ENSP00000514752.2:p.Arg1193Gly | |
| ENST00000699999.1:n.4635A>G (MSH6) | ||
| ENST00000700000.1:c.2395A>G (MSH6) | ENSP00000514749.1:p.Arg799Gly | |
| ENST00000700002.1:c.3967A>G (MSH6) | ENSP00000514750.1:p.Arg1323Gly | |
| ENST00000700003.1:c.1416A>G (MSH6) | ENSP00000514751.1:n.1416A>G | |
| ENST00000700004.1:c.2734A>G (MSH6) | ENSP00000514752.1:p.Arg912Gly | |
| ENST00000700005.1:n.2812A>G (MSH6) | ||
| ENST00000700006.1:n.5119A>G (MSH6) | ||
| ENST00000700007.1:n.2556A>G (MSH6) | ||
| ENST00000700008.1:n.2223A>G (MSH6) | ||
| ENST00000700009.1:n.2625A>G (MSH6) | ||
| ENST00000700010.1:n.1370A>G (MSH6) | ||
| ENST00000700011.1:n.3255A>G (MSH6) | ||
| ENST00000682451.1:n.4137T>C (FBXO11) | ||
| ENST00000684712.1:n.4399T>C (FBXO11) | ||
| ENST00000234420.11:c.3961A>G (MSH6) MANE Select | ENSP00000234420.5:p.Arg1321Gly | |
| ENST00000540021.6:c.3571A>G (MSH6) | ENSP00000446475.1:p.Arg1191Gly | |
| ENST00000652107.1:c.3664A>G (MSH6) | ENSP00000498629.1:p.Arg1222Gly | |
| ENST00000673637.1:c.3664A>G (MSH6) | ENSP00000501310.1:p.Arg1222Gly | |
| ENST00000234420.9:c.3961A>G (MSH6) | ENSP00000234420.4:p.Arg1321Gly | |
| ENST00000405808.5:c.169+1584T>C (FBXO11) | ENSP00000385127.1:n.169+1584T>C | |
| ENST00000434234.5:c.*124+1383T>C (FBXO11) | ENSP00000402692.1:n.*124+1383T>C | |
| ENST00000445503.5:c.*3308A>G (MSH6) | ENSP00000405294.1:n.*3308A>G | |
| ENST00000538136.1:c.3055A>G (MSH6) | ENSP00000438580.1:p.Arg1019Gly | |
| ENST00000540021.5:c.3571A>G (MSH6) | ENSP00000446475.1:p.Arg1191Gly | |
| ENST00000614496.4:c.3055A>G (MSH6) | ENSP00000477844.1:p.Arg1019Gly | |
| ENST00000622629.4:c.862A>G (MSH6) | ENSP00000482078.1:p.Arg288Gly | |
| NM_000179.2:c.3961A>G , LRG_219t1:c.3961A>G (MSH6) | NP_000170.1:p.Arg1321Gly | |
| NM_001281492.1:c.3571A>G (MSH6) | NP_001268421.1:p.Arg1191Gly | |
| NM_001281493.1:c.3055A>G (MSH6) | NP_001268422.1:p.Arg1019Gly | |
| NM_001281494.1:c.3055A>G (MSH6) | NP_001268423.1:p.Arg1019Gly | |
| XM_005264271.1:c.3664A>G (MSH6) | XP_005264328.1:p.Arg1222Gly | |
| XM_011532798.1:c.3778A>G (MSH6) | XP_011531100.1:p.Arg1260Gly | |
| XM_011532799.1:c.3664A>G (MSH6) | XP_011531101.1:p.Arg1222Gly | |
| XM_011532800.1:c.3664A>G (MSH6) | XP_011531102.1:p.Arg1222Gly | |
| XM_024452819.1:c.4054A>G (MSH6) | XP_024308587.1:p.Arg1352Gly | |
| XM_024452820.1:c.3871A>G (MSH6) | XP_024308588.1:p.Arg1291Gly | |
| XM_024452821.1:c.3757A>G (MSH6) | XP_024308589.1:p.Arg1253Gly | |
| XM_024452822.1:c.3148A>G (MSH6) | XP_024308590.1:p.Arg1050Gly | |
| NM_000179.3:c.3961A>G (MSH6) MANE Select | NP_000170.1:p.Arg1321Gly | |
| NM_001281492.2:c.3571A>G (MSH6) | NP_001268421.1:p.Arg1191Gly | |
| NM_001281493.2:c.3055A>G (MSH6) | NP_001268422.1:p.Arg1019Gly | |
| NM_001281494.2:c.3055A>G (MSH6) | NP_001268423.1:p.Arg1019Gly |