Linked Data
ClinVar Variation Id:
135836
dbSNP Id:
rs587780673
MyVariant Identifiers:
chr2:g.48027683_48027684delinsTT (hg19)
chr2:g.47800544_47800545delinsTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47800544_47800545delinsTT , CM000664.2:g.47800544_47800545delinsTT | GRCh38 |
| NC_000002.11:g.48027683_48027684delinsTT , CM000664.1:g.48027683_48027684delinsTT | GRCh37 |
| NC_000002.10:g.47881187_47881188delinsTT | NCBI36 |
| NG_007111.1:g.22398_22399delinsTT , LRG_219:g.22398_22399delinsTT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411819.2:c.2264_2265delinsTT (MSH6) | ENSP00000406248.2:p.Lys755Ile | |
| ENST00000420813.6:c.2264_2265delinsTT (MSH6) | ENSP00000390382.2:p.Lys755Ile | |
| ENST00000455383.6:c.2264_2265delinsTT (MSH6) | ENSP00000397484.2:p.Lys755Ile | |
| ENST00000700004.2:c.2561_2562delinsTT (MSH6) | ENSP00000514752.2:p.Lys854Ile | |
| ENST00000699999.1:n.2645_2646delinsTT (MSH6) | ||
| ENST00000700000.1:c.1606+955_1606+956delinsTT (MSH6) | ENSP00000514749.1:n.1606+955_1606+956deli... | |
| ENST00000700002.1:c.2567_2568delinsTT (MSH6) | ENSP00000514750.1:p.Lys856Ile | |
| ENST00000700003.1:c.628-2876_628-2875delinsTT (MSH6) | ENSP00000514751.1:n.628-2876_628-2875deli... | |
| ENST00000700004.1:c.1718_1719delinsTT (MSH6) | ENSP00000514752.1:p.Lys573Ile | |
| ENST00000234420.11:c.2561_2562delinsTT (MSH6) MANE Select | ENSP00000234420.5:p.Lys854Ile | |
| ENST00000540021.6:c.2171_2172delinsTT (MSH6) | ENSP00000446475.1:p.Lys724Ile | |
| ENST00000652107.1:c.2264_2265delinsTT (MSH6) | ENSP00000498629.1:p.Lys755Ile | |
| ENST00000673637.1:c.2264_2265delinsTT (MSH6) | ENSP00000501310.1:p.Lys755Ile | |
| ENST00000234420.9:c.2561_2562delinsTT (MSH6) | ENSP00000234420.4:p.Lys854Ile | |
| ENST00000405808.5:c.169+7650_169+7651delinsAA (FBXO11) | ENSP00000385127.1:n.169+7650_169+7651deli... | |
| ENST00000434234.5:c.*124+7449_*124+7450delinsAA (FBXO11) | ENSP00000402692.1:n.*124+7449_*124+7450de... | |
| ENST00000445503.5:c.*1908_*1909delinsTT (MSH6) | ENSP00000405294.1:n.*1908_*1909delinsTT | |
| ENST00000538136.1:c.1655_1656delinsTT (MSH6) | ENSP00000438580.1:p.Lys552Ile | |
| ENST00000540021.5:c.2171_2172delinsTT (MSH6) | ENSP00000446475.1:p.Lys724Ile | |
| ENST00000614496.4:c.1655_1656delinsTT (MSH6) | ENSP00000477844.1:p.Lys552Ile | |
| ENST00000616033.4:c.2558_2559delinsTT (MSH6) | ENSP00000480261.1:p.Lys853Ile | |
| ENST00000622629.4:c.-536_-535delinsTT (MSH6) | ENSP00000482078.1:n.-536_-535delinsTT | |
| NM_000179.2:c.2561_2562delinsTT , LRG_219t1:c.2561_2562delinsTT (MSH6) | NP_000170.1:p.Lys854Ile | |
| NM_001281492.1:c.2171_2172delinsTT (MSH6) | NP_001268421.1:p.Lys724Ile | |
| NM_001281493.1:c.1655_1656delinsTT (MSH6) | NP_001268422.1:p.Lys552Ile | |
| NM_001281494.1:c.1655_1656delinsTT (MSH6) | NP_001268423.1:p.Lys552Ile | |
| XM_005264271.1:c.2264_2265delinsTT (MSH6) | XP_005264328.1:p.Lys755Ile | |
| XM_011532798.1:c.2378_2379delinsTT (MSH6) | XP_011531100.1:p.Lys793Ile | |
| XM_011532799.1:c.2264_2265delinsTT (MSH6) | XP_011531101.1:p.Lys755Ile | |
| XM_011532800.1:c.2264_2265delinsTT (MSH6) | XP_011531102.1:p.Lys755Ile | |
| XM_024452819.1:c.2561_2562delinsTT (MSH6) | XP_024308587.1:p.Lys854Ile | |
| XM_024452820.1:c.2378_2379delinsTT (MSH6) | XP_024308588.1:p.Lys793Ile | |
| XM_024452821.1:c.2264_2265delinsTT (MSH6) | XP_024308589.1:p.Lys755Ile | |
| XM_024452822.1:c.1655_1656delinsTT (MSH6) | XP_024308590.1:p.Lys552Ile | |
| NM_000179.3:c.2561_2562delinsTT (MSH6) MANE Select | NP_000170.1:p.Lys854Ile | |
| NM_001281492.2:c.2171_2172delinsTT (MSH6) | NP_001268421.1:p.Lys724Ile | |
| NM_001281493.2:c.1655_1656delinsTT (MSH6) | NP_001268422.1:p.Lys552Ile | |
| NM_001281494.2:c.1655_1656delinsTT (MSH6) | NP_001268423.1:p.Lys552Ile |