Canonical Allele Identifier: CA2496053904

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806162_47806176delinsATTCCTTTGAGTTAC , CM000664.2:g.47806162_47806176delinsATTCCTTTGAGTTAC GRCh38
NC_000002.11:g.48033301_48033315delinsATTCCTTTGAGTTAC , CM000664.1:g.48033301_48033315delinsATTCCTTTGAGTTAC GRCh37
NC_000002.10:g.47886805_47886819delinsATTCCTTTGAGTTAC NCBI36
NG_007111.1:g.28016_28030delinsATTCCTTTGAGTTAC , LRG_219:g.28016_28030delinsATTCCTTTGAGTTAC
NG_008397.1:g.104500_104514delinsGTAACTCAAAGGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000406248.2:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
ENST00000420813.6:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000390382.2:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
ENST00000455383.6:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000397484.2:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
ENST00000700004.2:c.3263-42_3263-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000514752.2:n.3263-42_3263-28delinsATTCCTTTGAGTTAC
ENST00000699999.1:n.4321-42_4321-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700000.1:c.2081-42_2081-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000514749.1:n.2081-42_2081-28delinsATTCCTTTGAGTTAC
ENST00000700002.1:c.3653-42_3653-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000514750.1:n.3653-42_3653-28delinsATTCCTTTGAGTTAC
ENST00000700003.1:c.1102-42_1102-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000514751.1:n.1102-42_1102-28delinsATTCCTTTGAGTTAC
ENST00000700004.1:c.2420-42_2420-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000514752.1:n.2420-42_2420-28delinsATTCCTTTGAGTTAC
ENST00000700005.1:n.2498-42_2498-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700006.1:n.4763_4777delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700007.1:n.2242-42_2242-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700008.1:n.1816-42_1816-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700009.1:n.2269_2283delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700010.1:n.1056-42_1056-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000700011.1:n.2941-42_2941-28delinsATTCCTTTGAGTTAC (MSH6)
ENST00000682451.1:n.4572_4586delinsGTAACTCAAAGGAAT (FBXO11)
ENST00000684712.1:n.4834_4848delinsGTAACTCAAAGGAAT (FBXO11)
ENST00000234420.11:c.3647-42_3647-28delinsATTCCTTTGAGTTAC (MSH6) MANE Select ENSP00000234420.5:n.3647-42_3647-28delinsATTCCTTTGAGTTAC
ENST00000540021.6:c.3257-42_3257-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000446475.1:n.3257-42_3257-28delinsATTCCTTTGAGTTAC
ENST00000652107.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000498629.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
ENST00000673637.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000501310.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
ENST00000234420.9:c.3647-42_3647-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000234420.4:n.3647-42_3647-28delinsATTCCTTTGAGTTAC
ENST00000405808.5:c.169+2019_169+2033delinsGTAACTCAAAGGAAT (FBXO11) ENSP00000385127.1:n.169+2019_169+2033delinsGTAACTCAAAGGAAT
ENST00000434234.5:c.*124+1818_*124+1832delinsGTAACTCAAAGGAAT (FBXO11) ENSP00000402692.1:n.*124+1818_*124+1832delinsGTAACTCAAAGGAAT
ENST00000445503.5:c.*2994-42_*2994-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000405294.1:n.*2994-42_*2994-28delinsATTCCTTTGAGTTAC
ENST00000538136.1:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000438580.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
ENST00000540021.5:c.3257-42_3257-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000446475.1:n.3257-42_3257-28delinsATTCCTTTGAGTTAC
ENST00000614496.4:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000477844.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
ENST00000622629.4:c.551-42_551-28delinsATTCCTTTGAGTTAC (MSH6) ENSP00000482078.1:n.551-42_551-28delinsATTCCTTTGAGTTAC
NM_000179.2:c.3647-42_3647-28delinsATTCCTTTGAGTTAC , LRG_219t1:c.3647-42_3647-28delinsATTCCTTTGAGTTAC (MSH6) NP_000170.1:n.3647-42_3647-28delinsATTCCTTTGAGTTAC
NM_001281492.1:c.3257-42_3257-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268421.1:n.3257-42_3257-28delinsATTCCTTTGAGTTAC
NM_001281493.1:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268422.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
NM_001281494.1:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268423.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
XM_005264271.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) XP_005264328.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
XM_011532798.1:c.3464-42_3464-28delinsATTCCTTTGAGTTAC (MSH6) XP_011531100.1:n.3464-42_3464-28delinsATTCCTTTGAGTTAC
XM_011532799.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) XP_011531101.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
XM_011532800.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) XP_011531102.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
XM_024452819.1:c.3647-42_3647-28delinsATTCCTTTGAGTTAC (MSH6) XP_024308587.1:n.3647-42_3647-28delinsATTCCTTTGAGTTAC
XM_024452820.1:c.3464-42_3464-28delinsATTCCTTTGAGTTAC (MSH6) XP_024308588.1:n.3464-42_3464-28delinsATTCCTTTGAGTTAC
XM_024452821.1:c.3350-42_3350-28delinsATTCCTTTGAGTTAC (MSH6) XP_024308589.1:n.3350-42_3350-28delinsATTCCTTTGAGTTAC
XM_024452822.1:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) XP_024308590.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
NM_000179.3:c.3647-42_3647-28delinsATTCCTTTGAGTTAC (MSH6) MANE Select NP_000170.1:n.3647-42_3647-28delinsATTCCTTTGAGTTAC
NM_001281492.2:c.3257-42_3257-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268421.1:n.3257-42_3257-28delinsATTCCTTTGAGTTAC
NM_001281493.2:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268422.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC
NM_001281494.2:c.2741-42_2741-28delinsATTCCTTTGAGTTAC (MSH6) NP_001268423.1:n.2741-42_2741-28delinsATTCCTTTGAGTTAC