Canonical Allele Identifier: CA2496054125

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806285_47806320delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG , CM000664.2:g.47806285_47806320delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG	GRCh38
NC_000002.11:g.48033424_48033459delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG , CM000664.1:g.48033424_48033459delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG	GRCh37
NC_000002.10:g.47886928_47886963delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG	NCBI36
NG_007111.1:g.28139_28174delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG , LRG_219:g.28139_28174delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG
NG_008397.1:g.104356_104391delinsCTTCTACTAATGAATGGTAGTGAGTTGAAAATAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000406248.2:p.Thr1144=
ENST00000420813.6:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000390382.2:p.Thr1144=
ENST00000455383.6:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000397484.2:p.Thr1144=
ENST00000700004.2:c.3344_3379delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000514752.2:p.Thr1115=
ENST00000699999.1:n.4402_4437delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700000.1:c.2162_2197delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000514749.1:p.Thr721=
ENST00000700002.1:c.3734_3769delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000514750.1:p.Thr1245=
ENST00000700003.1:c.1183_1218delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000514751.1:n.1183_1218delinsCATTATTTTCAACTCACTACCATTCA...
ENST00000700004.1:c.2501_2536delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000514752.1:p.Thr834=
ENST00000700005.1:n.2579_2614delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700006.1:n.4886_4921delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700007.1:n.2323_2358delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700008.1:n.1897_1932delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700009.1:n.2392_2427delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700010.1:n.1137_1172delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000700011.1:n.3022_3057delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
ENST00000682451.1:n.4428_4463delinsCTTCTACTAATGAATGGTAGTGAGTTGAAAATAATG (FBXO11)
ENST00000684712.1:n.4690_4725delinsCTTCTACTAATGAATGGTAGTGAGTTGAAAATAATG (FBXO11)
ENST00000234420.11:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6) MANE Select	ENSP00000234420.5:p.Thr1243=
ENST00000540021.6:c.3338_3373delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000446475.1:p.Thr1113=
ENST00000652107.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000498629.1:p.Thr1144=
ENST00000673637.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000501310.1:p.Thr1144=
ENST00000234420.9:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000234420.4:p.Thr1243=
ENST00000405808.5:c.169+1875_169+1910delinsCTTCTACTAATGAATGGTAGTGAGTTGAAAATAATG (FBXO11)	ENSP00000385127.1:n.169+1875_169+1910delinsCTTCTACTAATGAATGGT...
ENST00000434234.5:c.*124+1674_*124+1709delinsCTTCTACTAATGAATGGTAGTGAGTTGAAAATAATG (FBXO11)	ENSP00000402692.1:n.*124+1674_*124+1709delinsCTTCTACTAATGAATG...
ENST00000445503.5:c.*3075_*3110delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000405294.1:n.*3075_*3110delinsCATTATTTTCAACTCACTACCATT...
ENST00000538136.1:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000438580.1:p.Thr941=
ENST00000540021.5:c.3338_3373delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000446475.1:p.Thr1113=
ENST00000614496.4:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	ENSP00000477844.1:p.Thr941=
ENST00000622629.4:c.632_665delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)
NM_000179.2:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG , LRG_219t1:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_000170.1:p.Thr1243=
NM_001281492.1:c.3338_3373delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268421.1:p.Thr1113=
NM_001281493.1:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268422.1:p.Thr941=
NM_001281494.1:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268423.1:p.Thr941=
XM_005264271.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_005264328.1:p.Thr1144=
XM_011532798.1:c.3545_3580delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_011531100.1:p.Thr1182=
XM_011532799.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_011531101.1:p.Thr1144=
XM_011532800.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_011531102.1:p.Thr1144=
XM_024452819.1:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_024308587.1:p.Thr1243=
XM_024452820.1:c.3545_3580delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_024308588.1:p.Thr1182=
XM_024452821.1:c.3431_3466delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_024308589.1:p.Thr1144=
XM_024452822.1:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	XP_024308590.1:p.Thr941=
NM_000179.3:c.3728_3763delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6) MANE Select	NP_000170.1:p.Thr1243=
NM_001281492.2:c.3338_3373delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268421.1:p.Thr1113=
NM_001281493.2:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268422.1:p.Thr941=
NM_001281494.2:c.2822_2857delinsCATTATTTTCAACTCACTACCATTCATTAGTAGAAG (MSH6)	NP_001268423.1:p.Thr941=