Linked Data
ClinVar Variation Id:
924399
ClinVar RCV Id:
RCV001185689
dbSNP Id:
rs1669315029
COSMIC:
COSM4568691
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47799262T>G , CM000664.2:g.47799262T>G | GRCh38 |
| NC_000002.11:g.48026401T>G , CM000664.1:g.48026401T>G | GRCh37 |
| NC_000002.10:g.47879905T>G | NCBI36 |
| NG_007111.1:g.21116T>G , LRG_219:g.21116T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.982T>G (MSH6) | ENSP00000406248.2:p.Tyr328Asp | |
| ENST00000420813.6:c.982T>G (MSH6) | ENSP00000390382.2:p.Tyr328Asp | |
| ENST00000455383.6:c.982T>G (MSH6) | ENSP00000397484.2:p.Tyr328Asp | |
| ENST00000700004.2:c.1279T>G (MSH6) | ENSP00000514752.2:p.Tyr427Asp | |
| ENST00000699999.1:n.1363T>G (MSH6) | ||
| ENST00000700000.1:c.1279T>G (MSH6) | ENSP00000514749.1:p.Tyr427Asp | |
| ENST00000700002.1:c.1285T>G (MSH6) | ENSP00000514750.1:p.Tyr429Asp | |
| ENST00000700003.1:c.627+3199T>G (MSH6) | ENSP00000514751.1:n.627+3199T>G | |
| ENST00000700004.1:c.436T>G (MSH6) | ENSP00000514752.1:p.Tyr146Asp | |
| ENST00000234420.11:c.1279T>G (MSH6) MANE Select | ENSP00000234420.5:p.Tyr427Asp | |
| ENST00000540021.6:c.889T>G (MSH6) | ENSP00000446475.1:p.Tyr297Asp | |
| ENST00000652107.1:c.982T>G (MSH6) | ENSP00000498629.1:p.Tyr328Asp | |
| ENST00000673637.1:c.982T>G (MSH6) | ENSP00000501310.1:p.Tyr328Asp | |
| ENST00000234420.9:c.1279T>G (MSH6) | ENSP00000234420.4:p.Tyr427Asp | |
| ENST00000405808.5:c.169+8933A>C (FBXO11) | ENSP00000385127.1:n.169+8933A>C | |
| ENST00000434234.5:c.*124+8732A>C (FBXO11) | ENSP00000402692.1:n.*124+8732A>C | |
| ENST00000445503.5:c.*626T>G (MSH6) | ENSP00000405294.1:n.*626T>G | |
| ENST00000538136.1:c.373T>G (MSH6) | ENSP00000438580.1:p.Tyr125Asp | |
| ENST00000540021.5:c.889T>G (MSH6) | ENSP00000446475.1:p.Tyr297Asp | |
| ENST00000614496.4:c.373T>G (MSH6) | ENSP00000477844.1:p.Tyr125Asp | |
| ENST00000616033.4:c.1276T>G (MSH6) | ENSP00000480261.1:p.Tyr426Asp | |
| ENST00000622629.4:c.-1818T>G (MSH6) | ENSP00000482078.1:n.-1818T>G | |
| NM_000179.2:c.1279T>G , LRG_219t1:c.1279T>G (MSH6) | NP_000170.1:p.Tyr427Asp | |
| NM_001281492.1:c.889T>G (MSH6) | NP_001268421.1:p.Tyr297Asp | |
| NM_001281493.1:c.373T>G (MSH6) | NP_001268422.1:p.Tyr125Asp | |
| NM_001281494.1:c.373T>G (MSH6) | NP_001268423.1:p.Tyr125Asp | |
| XM_005264271.1:c.982T>G (MSH6) | XP_005264328.1:p.Tyr328Asp | |
| XM_011532798.1:c.1096T>G (MSH6) | XP_011531100.1:p.Tyr366Asp | |
| XM_011532799.1:c.982T>G (MSH6) | XP_011531101.1:p.Tyr328Asp | |
| XM_011532800.1:c.982T>G (MSH6) | XP_011531102.1:p.Tyr328Asp | |
| XM_024452819.1:c.1279T>G (MSH6) | XP_024308587.1:p.Tyr427Asp | |
| XM_024452820.1:c.1096T>G (MSH6) | XP_024308588.1:p.Tyr366Asp | |
| XM_024452821.1:c.982T>G (MSH6) | XP_024308589.1:p.Tyr328Asp | |
| XM_024452822.1:c.373T>G (MSH6) | XP_024308590.1:p.Tyr125Asp | |
| NM_000179.3:c.1279T>G (MSH6) MANE Select | NP_000170.1:p.Tyr427Asp | |
| NM_001281492.2:c.889T>G (MSH6) | NP_001268421.1:p.Tyr297Asp | |
| NM_001281493.2:c.373T>G (MSH6) | NP_001268422.1:p.Tyr125Asp | |
| NM_001281494.2:c.373T>G (MSH6) | NP_001268423.1:p.Tyr125Asp |