Canonical Allele Identifier: CA1030296775

Linked Data

ClinVar Variation Id: 1392716
dbSNP Id: rs1670107768

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806512_47806532dup , CM000664.2:g.47806512_47806532dup GRCh38
NC_000002.11:g.48033651_48033671dup , CM000664.1:g.48033651_48033671dup GRCh37
NC_000002.10:g.47887155_47887175dup NCBI36
NG_007111.1:g.28366_28386dup , LRG_219:g.28366_28386dup
NG_008397.1:g.104145_104165dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3565_3585dup (MSH6) ENSP00000406248.2:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
ENST00000420813.6:c.3565_3585dup (MSH6) ENSP00000390382.2:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
ENST00000455383.6:c.3565_3585dup (MSH6) ENSP00000397484.2:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
ENST00000700004.2:c.3478_3498dup (MSH6) ENSP00000514752.2:p.Cys1166_Pro1167insLysPheIleLysGlyAlaCys
ENST00000699999.1:n.4536_4556dup (MSH6)
ENST00000700000.1:c.2296_2316dup (MSH6) ENSP00000514749.1:p.Cys772_Pro773insLysPheIleLysGlyAlaCys
ENST00000700002.1:c.3868_3888dup (MSH6) ENSP00000514750.1:p.Cys1296_Pro1297insLysPheIleLysGlyAlaCys
ENST00000700003.1:c.1317_1337dup (MSH6) ENSP00000514751.1:n.1317_1337dup
ENST00000700004.1:c.2635_2655dup (MSH6) ENSP00000514752.1:p.Cys885_Pro886insLysPheIleLysGlyAlaCys
ENST00000700005.1:n.2713_2733dup (MSH6)
ENST00000700006.1:n.5020_5040dup (MSH6)
ENST00000700007.1:n.2457_2477dup (MSH6)
ENST00000700008.1:n.2124_2144dup (MSH6)
ENST00000700009.1:n.2526_2546dup (MSH6)
ENST00000700010.1:n.1271_1291dup (MSH6)
ENST00000700011.1:n.3156_3176dup (MSH6)
ENST00000682451.1:n.4217_4237dup (FBXO11)
ENST00000684712.1:n.4479_4499dup (FBXO11)
ENST00000234420.11:c.3862_3882dup (MSH6) MANE Select ENSP00000234420.5:p.Cys1294_Pro1295insLysPheIleLysGlyAlaCys
ENST00000540021.6:c.3472_3492dup (MSH6) ENSP00000446475.1:p.Cys1164_Pro1165insLysPheIleLysGlyAlaCys
ENST00000652107.1:c.3565_3585dup (MSH6) ENSP00000498629.1:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
ENST00000673637.1:c.3565_3585dup (MSH6) ENSP00000501310.1:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
ENST00000234420.9:c.3862_3882dup (MSH6) ENSP00000234420.4:p.Cys1294_Pro1295insLysPheIleLysGlyAlaCys
ENST00000405808.5:c.169+1664_169+1684dup (FBXO11) ENSP00000385127.1:n.169+1664_169+1684dup
ENST00000434234.5:c.*124+1463_*124+1483dup (FBXO11) ENSP00000402692.1:n.*124+1463_*124+1483dup
ENST00000445503.5:c.*3209_*3229dup (MSH6) ENSP00000405294.1:n.*3209_*3229dup
ENST00000538136.1:c.2956_2976dup (MSH6) ENSP00000438580.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys
ENST00000540021.5:c.3472_3492dup (MSH6) ENSP00000446475.1:p.Cys1164_Pro1165insLysPheIleLysGlyAlaCys
ENST00000614496.4:c.2956_2976dup (MSH6) ENSP00000477844.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys
ENST00000622629.4:c.763_783dup (MSH6) ENSP00000482078.1:p.Cys261_Pro262insLysPheIleLysGlyAlaCys
NM_000179.2:c.3862_3882dup , LRG_219t1:c.3862_3882dup (MSH6) NP_000170.1:p.Cys1294_Pro1295insLysPheIleLysGlyAlaCys
NM_001281492.1:c.3472_3492dup (MSH6) NP_001268421.1:p.Cys1164_Pro1165insLysPheIleLysGlyAlaCys
NM_001281493.1:c.2956_2976dup (MSH6) NP_001268422.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys
NM_001281494.1:c.2956_2976dup (MSH6) NP_001268423.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys
XM_005264271.1:c.3565_3585dup (MSH6) XP_005264328.1:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
XM_011532798.1:c.3679_3699dup (MSH6) XP_011531100.1:p.Cys1233_Pro1234insLysPheIleLysGlyAlaCys
XM_011532799.1:c.3565_3585dup (MSH6) XP_011531101.1:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
XM_011532800.1:c.3565_3585dup (MSH6) XP_011531102.1:p.Cys1195_Pro1196insLysPheIleLysGlyAlaCys
XM_024452819.1:c.3955_3975dup (MSH6) XP_024308587.1:p.Cys1325_Pro1326insLysPheIleLysGlyAlaCys
XM_024452820.1:c.3772_3792dup (MSH6) XP_024308588.1:p.Cys1264_Pro1265insLysPheIleLysGlyAlaCys
XM_024452821.1:c.3658_3678dup (MSH6) XP_024308589.1:p.Cys1226_Pro1227insLysPheIleLysGlyAlaCys
XM_024452822.1:c.3049_3069dup (MSH6) XP_024308590.1:p.Cys1023_Pro1024insLysPheIleLysGlyAlaCys
NM_000179.3:c.3862_3882dup (MSH6) MANE Select NP_000170.1:p.Cys1294_Pro1295insLysPheIleLysGlyAlaCys
NM_001281492.2:c.3472_3492dup (MSH6) NP_001268421.1:p.Cys1164_Pro1165insLysPheIleLysGlyAlaCys
NM_001281493.2:c.2956_2976dup (MSH6) NP_001268422.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys
NM_001281494.2:c.2956_2976dup (MSH6) NP_001268423.1:p.Cys992_Pro993insLysPheIleLysGlyAlaCys