Canonical Allele Identifier: CA2496054392

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806668_47806682delinsAATGGAATTATAACT , CM000664.2:g.47806668_47806682delinsAATGGAATTATAACT	GRCh38
NC_000002.11:g.48033807_48033821delinsAATGGAATTATAACT , CM000664.1:g.48033807_48033821delinsAATGGAATTATAACT	GRCh37
NC_000002.10:g.47887311_47887325delinsAATGGAATTATAACT	NCBI36
NG_007111.1:g.28522_28536delinsAATGGAATTATAACT , LRG_219:g.28522_28536delinsAATGGAATTATAACT
NG_008397.1:g.103994_104008delinsAGTTATAATTCCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	ENSP00000406248.2:n.3704+17_3704+31delinsAATGGAATTATAACT
ENST00000420813.6:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	ENSP00000390382.2:n.3704+17_3704+31delinsAATGGAATTATAACT
ENST00000455383.6:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	ENSP00000397484.2:n.3704+17_3704+31delinsAATGGAATTATAACT
ENST00000700004.2:c.3617+17_3617+31delinsAATGGAATTATAACT (MSH6)	ENSP00000514752.2:n.3617+17_3617+31delinsAATGGAATTATAACT
ENST00000699999.1:n.4675+17_4675+31delinsAATGGAATTATAACT (MSH6)
ENST00000700000.1:c.2435+17_2435+31delinsAATGGAATTATAACT (MSH6)	ENSP00000514749.1:n.2435+17_2435+31delinsAATGGAATTATAACT
ENST00000700002.1:c.4007+17_4007+31delinsAATGGAATTATAACT (MSH6)	ENSP00000514750.1:n.4007+17_4007+31delinsAATGGAATTATAACT
ENST00000700003.1:c.1456+17_1456+31delinsAATGGAATTATAACT (MSH6)	ENSP00000514751.1:n.1456+17_1456+31delinsAATGGAATTATAACT
ENST00000700004.1:c.2774+17_2774+31delinsAATGGAATTATAACT (MSH6)	ENSP00000514752.1:n.2774+17_2774+31delinsAATGGAATTATAACT
ENST00000700005.1:n.2869_2883delinsAATGGAATTATAACT (MSH6)
ENST00000700006.1:n.5176_5190delinsAATGGAATTATAACT (MSH6)
ENST00000700007.1:n.2596+17_2596+31delinsAATGGAATTATAACT (MSH6)
ENST00000700008.1:n.2263+17_2263+31delinsAATGGAATTATAACT (MSH6)
ENST00000700009.1:n.2665+17_2665+31delinsAATGGAATTATAACT (MSH6)
ENST00000700010.1:n.1410+17_1410+31delinsAATGGAATTATAACT (MSH6)
ENST00000700011.1:n.3295+17_3295+31delinsAATGGAATTATAACT (MSH6)
ENST00000682451.1:n.4066_4080delinsAGTTATAATTCCATT (FBXO11)
ENST00000684712.1:n.4328_4342delinsAGTTATAATTCCATT (FBXO11)
ENST00000234420.11:c.4001+17_4001+31delinsAATGGAATTATAACT (MSH6) MANE Select	ENSP00000234420.5:n.4001+17_4001+31delinsAATGGAATTATAACT
ENST00000540021.6:c.3611+17_3611+31delinsAATGGAATTATAACT (MSH6)	ENSP00000446475.1:n.3611+17_3611+31delinsAATGGAATTATAACT
ENST00000652107.1:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	ENSP00000498629.1:n.3704+17_3704+31delinsAATGGAATTATAACT
ENST00000673637.1:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	ENSP00000501310.1:n.3704+17_3704+31delinsAATGGAATTATAACT
ENST00000234420.9:c.4001+17_4001+31delinsAATGGAATTATAACT (MSH6)	ENSP00000234420.4:n.4001+17_4001+31delinsAATGGAATTATAACT
ENST00000405808.5:c.169+1513_169+1527delinsAGTTATAATTCCATT (FBXO11)	ENSP00000385127.1:n.169+1513_169+1527delinsAGTTATAATTCCATT
ENST00000434234.5:c.*124+1312_*124+1326delinsAGTTATAATTCCATT (FBXO11)	ENSP00000402692.1:n.*124+1312_*124+1326delinsAGTTATAATTCCATT
ENST00000445503.5:c.*3348+17_*3348+31delinsAATGGAATTATAACT (MSH6)	ENSP00000405294.1:n.*3348+17_*3348+31delinsAATGGAATTATAACT
ENST00000538136.1:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	ENSP00000438580.1:n.3095+17_3095+31delinsAATGGAATTATAACT
ENST00000540021.5:c.3611+17_3611+31delinsAATGGAATTATAACT (MSH6)	ENSP00000446475.1:n.3611+17_3611+31delinsAATGGAATTATAACT
ENST00000614496.4:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	ENSP00000477844.1:n.3095+17_3095+31delinsAATGGAATTATAACT
ENST00000622629.4:c.902+17_902+31delinsAATGGAATTATAACT (MSH6)	ENSP00000482078.1:n.902+17_902+31delinsAATGGAATTATAACT
NM_000179.2:c.4001+17_4001+31delinsAATGGAATTATAACT , LRG_219t1:c.4001+17_4001+31delinsAATGGAATTATAACT (MSH6)	NP_000170.1:n.4001+17_4001+31delinsAATGGAATTATAACT
NM_001281492.1:c.3611+17_3611+31delinsAATGGAATTATAACT (MSH6)	NP_001268421.1:n.3611+17_3611+31delinsAATGGAATTATAACT
NM_001281493.1:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	NP_001268422.1:n.3095+17_3095+31delinsAATGGAATTATAACT
NM_001281494.1:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	NP_001268423.1:n.3095+17_3095+31delinsAATGGAATTATAACT
XM_005264271.1:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	XP_005264328.1:n.3704+17_3704+31delinsAATGGAATTATAACT
XM_011532798.1:c.3818+17_3818+31delinsAATGGAATTATAACT (MSH6)	XP_011531100.1:n.3818+17_3818+31delinsAATGGAATTATAACT
XM_011532799.1:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	XP_011531101.1:n.3704+17_3704+31delinsAATGGAATTATAACT
XM_011532800.1:c.3704+17_3704+31delinsAATGGAATTATAACT (MSH6)	XP_011531102.1:n.3704+17_3704+31delinsAATGGAATTATAACT
XM_024452819.1:c.4094+17_4094+31delinsAATGGAATTATAACT (MSH6)	XP_024308587.1:n.4094+17_4094+31delinsAATGGAATTATAACT
XM_024452820.1:c.3911+17_3911+31delinsAATGGAATTATAACT (MSH6)	XP_024308588.1:n.3911+17_3911+31delinsAATGGAATTATAACT
XM_024452821.1:c.3797+17_3797+31delinsAATGGAATTATAACT (MSH6)	XP_024308589.1:n.3797+17_3797+31delinsAATGGAATTATAACT
XM_024452822.1:c.3188+17_3188+31delinsAATGGAATTATAACT (MSH6)	XP_024308590.1:n.3188+17_3188+31delinsAATGGAATTATAACT
NM_000179.3:c.4001+17_4001+31delinsAATGGAATTATAACT (MSH6) MANE Select	NP_000170.1:n.4001+17_4001+31delinsAATGGAATTATAACT
NM_001281492.2:c.3611+17_3611+31delinsAATGGAATTATAACT (MSH6)	NP_001268421.1:n.3611+17_3611+31delinsAATGGAATTATAACT
NM_001281493.2:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	NP_001268422.1:n.3095+17_3095+31delinsAATGGAATTATAACT
NM_001281494.2:c.3095+17_3095+31delinsAATGGAATTATAACT (MSH6)	NP_001268423.1:n.3095+17_3095+31delinsAATGGAATTATAACT