Canonical Allele Identifier: CA2496054280

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806565_47806580delinsTGCTAATCTCCCAGAG , CM000664.2:g.47806565_47806580delinsTGCTAATCTCCCAGAG GRCh38
NC_000002.11:g.48033704_48033719delinsTGCTAATCTCCCAGAG , CM000664.1:g.48033704_48033719delinsTGCTAATCTCCCAGAG GRCh37
NC_000002.10:g.47887208_47887223delinsTGCTAATCTCCCAGAG NCBI36
NG_007111.1:g.28419_28434delinsTGCTAATCTCCCAGAG , LRG_219:g.28419_28434delinsTGCTAATCTCCCAGAG
NG_008397.1:g.104096_104111delinsCTCTGGGAGATTAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000406248.2:p.Leu1206=
ENST00000420813.6:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000390382.2:p.Leu1206=
ENST00000455383.6:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000397484.2:p.Leu1206=
ENST00000700004.2:c.3531_3546delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000514752.2:p.Leu1177=
ENST00000699999.1:n.4589_4604delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700000.1:c.2349_2364delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000514749.1:p.Leu783=
ENST00000700002.1:c.3921_3936delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000514750.1:p.Leu1307=
ENST00000700003.1:c.1370_1385delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000514751.1:n.1370_1385delinsTGCTAATCTCCCAGAG
ENST00000700004.1:c.2688_2703delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000514752.1:p.Leu896=
ENST00000700005.1:n.2766_2781delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700006.1:n.5073_5088delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700007.1:n.2510_2525delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700008.1:n.2177_2192delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700009.1:n.2579_2594delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700010.1:n.1324_1339delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000700011.1:n.3209_3224delinsTGCTAATCTCCCAGAG (MSH6)
ENST00000682451.1:n.4168_4183delinsCTCTGGGAGATTAGCA (FBXO11)
ENST00000684712.1:n.4430_4445delinsCTCTGGGAGATTAGCA (FBXO11)
ENST00000234420.11:c.3915_3930delinsTGCTAATCTCCCAGAG (MSH6) MANE Select ENSP00000234420.5:p.Leu1305=
ENST00000540021.6:c.3525_3540delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000446475.1:p.Leu1175=
ENST00000652107.1:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000498629.1:p.Leu1206=
ENST00000673637.1:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000501310.1:p.Leu1206=
ENST00000234420.9:c.3915_3930delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000234420.4:p.Leu1305=
ENST00000405808.5:c.169+1615_169+1630delinsCTCTGGGAGATTAGCA (FBXO11) ENSP00000385127.1:n.169+1615_169+1630delinsCTCTGGGAGATTAGCA
ENST00000434234.5:c.*124+1414_*124+1429delinsCTCTGGGAGATTAGCA (FBXO11) ENSP00000402692.1:n.*124+1414_*124+1429delinsCTCTGGGAGATTAGCA...
ENST00000445503.5:c.*3262_*3277delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000405294.1:n.*3262_*3277delinsTGCTAATCTCCCAGAG
ENST00000538136.1:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000438580.1:p.Leu1003=
ENST00000540021.5:c.3525_3540delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000446475.1:p.Leu1175=
ENST00000614496.4:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000477844.1:p.Leu1003=
ENST00000622629.4:c.816_831delinsTGCTAATCTCCCAGAG (MSH6) ENSP00000482078.1:p.Leu272=
NM_000179.2:c.3915_3930delinsTGCTAATCTCCCAGAG , LRG_219t1:c.3915_3930delinsTGCTAATCTCCCAGAG (MSH6) NP_000170.1:p.Leu1305=
NM_001281492.1:c.3525_3540delinsTGCTAATCTCCCAGAG (MSH6) NP_001268421.1:p.Leu1175=
NM_001281493.1:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) NP_001268422.1:p.Leu1003=
NM_001281494.1:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) NP_001268423.1:p.Leu1003=
XM_005264271.1:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) XP_005264328.1:p.Leu1206=
XM_011532798.1:c.3732_3747delinsTGCTAATCTCCCAGAG (MSH6) XP_011531100.1:p.Leu1244=
XM_011532799.1:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) XP_011531101.1:p.Leu1206=
XM_011532800.1:c.3618_3633delinsTGCTAATCTCCCAGAG (MSH6) XP_011531102.1:p.Leu1206=
XM_024452819.1:c.4008_4023delinsTGCTAATCTCCCAGAG (MSH6) XP_024308587.1:p.Leu1336=
XM_024452820.1:c.3825_3840delinsTGCTAATCTCCCAGAG (MSH6) XP_024308588.1:p.Leu1275=
XM_024452821.1:c.3711_3726delinsTGCTAATCTCCCAGAG (MSH6) XP_024308589.1:p.Leu1237=
XM_024452822.1:c.3102_3117delinsTGCTAATCTCCCAGAG (MSH6) XP_024308590.1:p.Leu1034=
NM_000179.3:c.3915_3930delinsTGCTAATCTCCCAGAG (MSH6) MANE Select NP_000170.1:p.Leu1305=
NM_001281492.2:c.3525_3540delinsTGCTAATCTCCCAGAG (MSH6) NP_001268421.1:p.Leu1175=
NM_001281493.2:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) NP_001268422.1:p.Leu1003=
NM_001281494.2:c.3009_3024delinsTGCTAATCTCCCAGAG (MSH6) NP_001268423.1:p.Leu1003=