Canonical Allele Identifier: CA346761229

Linked Data

ClinVar Variation Id: 1719480
ClinVar RCV Id: RCV002303753
dbSNP Id: rs770929545

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806461G>T , CM000664.2:g.47806461G>T GRCh38
NC_000002.11:g.48033600G>T , CM000664.1:g.48033600G>T GRCh37
NC_000002.10:g.47887104G>T NCBI36
NG_007111.1:g.28315G>T , LRG_219:g.28315G>T
NG_008397.1:g.104215C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3514G>T (MSH6) ENSP00000406248.2:p.Val1172Leu
ENST00000420813.6:c.3514G>T (MSH6) ENSP00000390382.2:p.Val1172Leu
ENST00000455383.6:c.3514G>T (MSH6) ENSP00000397484.2:p.Val1172Leu
ENST00000700004.2:c.3427G>T (MSH6) ENSP00000514752.2:p.Val1143Leu
ENST00000699999.1:n.4485G>T (MSH6)
ENST00000700000.1:c.2245G>T (MSH6) ENSP00000514749.1:p.Val749Leu
ENST00000700002.1:c.3817G>T (MSH6) ENSP00000514750.1:p.Val1273Leu
ENST00000700003.1:c.1266G>T (MSH6) ENSP00000514751.1:n.1266G>T
ENST00000700004.1:c.2584G>T (MSH6) ENSP00000514752.1:p.Val862Leu
ENST00000700005.1:n.2662G>T (MSH6)
ENST00000700006.1:n.4969G>T (MSH6)
ENST00000700007.1:n.2406G>T (MSH6)
ENST00000700008.1:n.2073G>T (MSH6)
ENST00000700009.1:n.2475G>T (MSH6)
ENST00000700010.1:n.1220G>T (MSH6)
ENST00000700011.1:n.3105G>T (MSH6)
ENST00000682451.1:n.4287C>A (FBXO11)
ENST00000684712.1:n.4549C>A (FBXO11)
ENST00000234420.11:c.3811G>T (MSH6) MANE Select ENSP00000234420.5:p.Val1271Leu
ENST00000540021.6:c.3421G>T (MSH6) ENSP00000446475.1:p.Val1141Leu
ENST00000652107.1:c.3514G>T (MSH6) ENSP00000498629.1:p.Val1172Leu
ENST00000673637.1:c.3514G>T (MSH6) ENSP00000501310.1:p.Val1172Leu
ENST00000234420.9:c.3811G>T (MSH6) ENSP00000234420.4:p.Val1271Leu
ENST00000405808.5:c.169+1734C>A (FBXO11) ENSP00000385127.1:n.169+1734C>A
ENST00000434234.5:c.*124+1533C>A (FBXO11) ENSP00000402692.1:n.*124+1533C>A
ENST00000445503.5:c.*3158G>T (MSH6) ENSP00000405294.1:n.*3158G>T
ENST00000538136.1:c.2905G>T (MSH6) ENSP00000438580.1:p.Val969Leu
ENST00000540021.5:c.3421G>T (MSH6) ENSP00000446475.1:p.Val1141Leu
ENST00000614496.4:c.2905G>T (MSH6) ENSP00000477844.1:p.Val969Leu
ENST00000622629.4:c.712G>T (MSH6) ENSP00000482078.1:p.Val238Leu
NM_000179.2:c.3811G>T , LRG_219t1:c.3811G>T (MSH6) NP_000170.1:p.Val1271Leu
NM_001281492.1:c.3421G>T (MSH6) NP_001268421.1:p.Val1141Leu
NM_001281493.1:c.2905G>T (MSH6) NP_001268422.1:p.Val969Leu
NM_001281494.1:c.2905G>T (MSH6) NP_001268423.1:p.Val969Leu
XM_005264271.1:c.3514G>T (MSH6) XP_005264328.1:p.Val1172Leu
XM_011532798.1:c.3628G>T (MSH6) XP_011531100.1:p.Val1210Leu
XM_011532799.1:c.3514G>T (MSH6) XP_011531101.1:p.Val1172Leu
XM_011532800.1:c.3514G>T (MSH6) XP_011531102.1:p.Val1172Leu
XM_024452819.1:c.3904G>T (MSH6) XP_024308587.1:p.Val1302Leu
XM_024452820.1:c.3721G>T (MSH6) XP_024308588.1:p.Val1241Leu
XM_024452821.1:c.3607G>T (MSH6) XP_024308589.1:p.Val1203Leu
XM_024452822.1:c.2998G>T (MSH6) XP_024308590.1:p.Val1000Leu
NM_000179.3:c.3811G>T (MSH6) MANE Select NP_000170.1:p.Val1271Leu
NM_001281492.2:c.3421G>T (MSH6) NP_001268421.1:p.Val1141Leu
NM_001281493.2:c.2905G>T (MSH6) NP_001268422.1:p.Val969Leu
NM_001281494.2:c.2905G>T (MSH6) NP_001268423.1:p.Val969Leu