Linked Data
ClinVar Variation Id:
1321051
dbSNP Id:
rs1201347192
gnomAD v2:
2-48027184-G-T
gnomAD v4:
2-47800045-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47800045G>T , CM000664.2:g.47800045G>T | GRCh38 |
| NC_000002.11:g.48027184G>T , CM000664.1:g.48027184G>T | GRCh37 |
| NC_000002.10:g.47880688G>T | NCBI36 |
| NG_007111.1:g.21899G>T , LRG_219:g.21899G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.1765G>T (MSH6) | ENSP00000406248.2:p.Val589Phe | |
| ENST00000420813.6:c.1765G>T (MSH6) | ENSP00000390382.2:p.Val589Phe | |
| ENST00000455383.6:c.1765G>T (MSH6) | ENSP00000397484.2:p.Val589Phe | |
| ENST00000700004.2:c.2062G>T (MSH6) | ENSP00000514752.2:p.Val688Phe | |
| ENST00000699999.1:n.2146G>T (MSH6) | ||
| ENST00000700000.1:c.1606+456G>T (MSH6) | ENSP00000514749.1:n.1606+456G>T | |
| ENST00000700002.1:c.2068G>T (MSH6) | ENSP00000514750.1:p.Val690Phe | |
| ENST00000700003.1:c.628-3375G>T (MSH6) | ENSP00000514751.1:n.628-3375G>T | |
| ENST00000700004.1:c.1219G>T (MSH6) | ENSP00000514752.1:p.Val407Phe | |
| ENST00000234420.11:c.2062G>T (MSH6) MANE Select | ENSP00000234420.5:p.Val688Phe | |
| ENST00000540021.6:c.1672G>T (MSH6) | ENSP00000446475.1:p.Val558Phe | |
| ENST00000652107.1:c.1765G>T (MSH6) | ENSP00000498629.1:p.Val589Phe | |
| ENST00000673637.1:c.1765G>T (MSH6) | ENSP00000501310.1:p.Val589Phe | |
| ENST00000234420.9:c.2062G>T (MSH6) | ENSP00000234420.4:p.Val688Phe | |
| ENST00000405808.5:c.169+8150C>A (FBXO11) | ENSP00000385127.1:n.169+8150C>A | |
| ENST00000434234.5:c.*124+7949C>A (FBXO11) | ENSP00000402692.1:n.*124+7949C>A | |
| ENST00000445503.5:c.*1409G>T (MSH6) | ENSP00000405294.1:n.*1409G>T | |
| ENST00000538136.1:c.1156G>T (MSH6) | ENSP00000438580.1:p.Val386Phe | |
| ENST00000540021.5:c.1672G>T (MSH6) | ENSP00000446475.1:p.Val558Phe | |
| ENST00000614496.4:c.1156G>T (MSH6) | ENSP00000477844.1:p.Val386Phe | |
| ENST00000616033.4:c.2059G>T (MSH6) | ENSP00000480261.1:p.Val687Phe | |
| ENST00000622629.4:c.-1035G>T (MSH6) | ENSP00000482078.1:n.-1035G>T | |
| NM_000179.2:c.2062G>T , LRG_219t1:c.2062G>T (MSH6) | NP_000170.1:p.Val688Phe | |
| NM_001281492.1:c.1672G>T (MSH6) | NP_001268421.1:p.Val558Phe | |
| NM_001281493.1:c.1156G>T (MSH6) | NP_001268422.1:p.Val386Phe | |
| NM_001281494.1:c.1156G>T (MSH6) | NP_001268423.1:p.Val386Phe | |
| XM_005264271.1:c.1765G>T (MSH6) | XP_005264328.1:p.Val589Phe | |
| XM_011532798.1:c.1879G>T (MSH6) | XP_011531100.1:p.Val627Phe | |
| XM_011532799.1:c.1765G>T (MSH6) | XP_011531101.1:p.Val589Phe | |
| XM_011532800.1:c.1765G>T (MSH6) | XP_011531102.1:p.Val589Phe | |
| XM_024452819.1:c.2062G>T (MSH6) | XP_024308587.1:p.Val688Phe | |
| XM_024452820.1:c.1879G>T (MSH6) | XP_024308588.1:p.Val627Phe | |
| XM_024452821.1:c.1765G>T (MSH6) | XP_024308589.1:p.Val589Phe | |
| XM_024452822.1:c.1156G>T (MSH6) | XP_024308590.1:p.Val386Phe | |
| NM_000179.3:c.2062G>T (MSH6) MANE Select | NP_000170.1:p.Val688Phe | |
| NM_001281492.2:c.1672G>T (MSH6) | NP_001268421.1:p.Val558Phe | |
| NM_001281493.2:c.1156G>T (MSH6) | NP_001268422.1:p.Val386Phe | |
| NM_001281494.2:c.1156G>T (MSH6) | NP_001268423.1:p.Val386Phe |