Canonical Allele Identifier: CA2496054430

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806705_47806709delinsAACAG , CM000664.2:g.47806705_47806709delinsAACAG	GRCh38
NC_000002.11:g.48033844_48033848delinsAACAG , CM000664.1:g.48033844_48033848delinsAACAG	GRCh37
NC_000002.10:g.47887348_47887352delinsAACAG	NCBI36
NG_007111.1:g.28559_28563delinsAACAG , LRG_219:g.28559_28563delinsAACAG
NG_008397.1:g.103967_103971delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+54_3704+58delinsAACAG (MSH6)	ENSP00000406248.2:n.3704+54_3704+58delinsAACAG
ENST00000420813.6:c.3704+54_3704+58delinsAACAG (MSH6)	ENSP00000390382.2:n.3704+54_3704+58delinsAACAG
ENST00000455383.6:c.3704+54_3704+58delinsAACAG (MSH6)	ENSP00000397484.2:n.3704+54_3704+58delinsAACAG
ENST00000700004.2:c.3617+54_3617+58delinsAACAG (MSH6)	ENSP00000514752.2:n.3617+54_3617+58delinsAACAG
ENST00000699999.1:n.4675+54_4675+58delinsAACAG (MSH6)
ENST00000700000.1:c.2435+54_2435+58delinsAACAG (MSH6)	ENSP00000514749.1:n.2435+54_2435+58delinsAACAG
ENST00000700002.1:c.4007+54_4007+58delinsAACAG (MSH6)	ENSP00000514750.1:n.4007+54_4007+58delinsAACAG
ENST00000700003.1:c.1456+54_1456+58delinsAACAG (MSH6)	ENSP00000514751.1:n.1456+54_1456+58delinsAACAG
ENST00000700004.1:c.2774+54_2774+58delinsAACAG (MSH6)	ENSP00000514752.1:n.2774+54_2774+58delinsAACAG
ENST00000700005.1:n.2906_2910delinsAACAG (MSH6)
ENST00000700006.1:n.5213_5217delinsAACAG (MSH6)
ENST00000700007.1:n.2596+54_2596+58delinsAACAG (MSH6)
ENST00000700008.1:n.2263+54_2263+58delinsAACAG (MSH6)
ENST00000700009.1:n.2665+54_2665+58delinsAACAG (MSH6)
ENST00000700010.1:n.1410+54_1410+58delinsAACAG (MSH6)
ENST00000700011.1:n.3295+54_3295+58delinsAACAG (MSH6)
ENST00000682451.1:n.4039_4043delinsCTGTT (FBXO11)
ENST00000684712.1:n.4301_4305delinsCTGTT (FBXO11)
ENST00000234420.11:c.4001+54_4001+58delinsAACAG (MSH6) MANE Select	ENSP00000234420.5:n.4001+54_4001+58delinsAACAG
ENST00000540021.6:c.3611+54_3611+58delinsAACAG (MSH6)	ENSP00000446475.1:n.3611+54_3611+58delinsAACAG
ENST00000652107.1:c.3704+54_3704+58delinsAACAG (MSH6)	ENSP00000498629.1:n.3704+54_3704+58delinsAACAG
ENST00000673637.1:c.3704+54_3704+58delinsAACAG (MSH6)	ENSP00000501310.1:n.3704+54_3704+58delinsAACAG
ENST00000234420.9:c.4001+54_4001+58delinsAACAG (MSH6)	ENSP00000234420.4:n.4001+54_4001+58delinsAACAG
ENST00000405808.5:c.169+1486_169+1490delinsCTGTT (FBXO11)	ENSP00000385127.1:n.169+1486_169+1490delinsCTGTT
ENST00000434234.5:c.*124+1285_*124+1289delinsCTGTT (FBXO11)	ENSP00000402692.1:n.*124+1285_*124+1289delinsCTGTT
ENST00000445503.5:c.*3348+54_*3348+58delinsAACAG (MSH6)	ENSP00000405294.1:n.*3348+54_*3348+58delinsAACAG
ENST00000538136.1:c.3095+54_3095+58delinsAACAG (MSH6)	ENSP00000438580.1:n.3095+54_3095+58delinsAACAG
ENST00000540021.5:c.3611+54_3611+58delinsAACAG (MSH6)	ENSP00000446475.1:n.3611+54_3611+58delinsAACAG
ENST00000614496.4:c.3095+54_3095+58delinsAACAG (MSH6)	ENSP00000477844.1:n.3095+54_3095+58delinsAACAG
ENST00000622629.4:c.902+54_902+58delinsAACAG (MSH6)	ENSP00000482078.1:n.902+54_902+58delinsAACAG
NM_000179.2:c.4001+54_4001+58delinsAACAG , LRG_219t1:c.4001+54_4001+58delinsAACAG (MSH6)	NP_000170.1:n.4001+54_4001+58delinsAACAG
NM_001281492.1:c.3611+54_3611+58delinsAACAG (MSH6)	NP_001268421.1:n.3611+54_3611+58delinsAACAG
NM_001281493.1:c.3095+54_3095+58delinsAACAG (MSH6)	NP_001268422.1:n.3095+54_3095+58delinsAACAG
NM_001281494.1:c.3095+54_3095+58delinsAACAG (MSH6)	NP_001268423.1:n.3095+54_3095+58delinsAACAG
XM_005264271.1:c.3704+54_3704+58delinsAACAG (MSH6)	XP_005264328.1:n.3704+54_3704+58delinsAACAG
XM_011532798.1:c.3818+54_3818+58delinsAACAG (MSH6)	XP_011531100.1:n.3818+54_3818+58delinsAACAG
XM_011532799.1:c.3704+54_3704+58delinsAACAG (MSH6)	XP_011531101.1:n.3704+54_3704+58delinsAACAG
XM_011532800.1:c.3704+54_3704+58delinsAACAG (MSH6)	XP_011531102.1:n.3704+54_3704+58delinsAACAG
XM_024452819.1:c.4094+54_4094+58delinsAACAG (MSH6)	XP_024308587.1:n.4094+54_4094+58delinsAACAG
XM_024452820.1:c.3911+54_3911+58delinsAACAG (MSH6)	XP_024308588.1:n.3911+54_3911+58delinsAACAG
XM_024452821.1:c.3797+54_3797+58delinsAACAG (MSH6)	XP_024308589.1:n.3797+54_3797+58delinsAACAG
XM_024452822.1:c.3188+54_3188+58delinsAACAG (MSH6)	XP_024308590.1:n.3188+54_3188+58delinsAACAG
NM_000179.3:c.4001+54_4001+58delinsAACAG (MSH6) MANE Select	NP_000170.1:n.4001+54_4001+58delinsAACAG
NM_001281492.2:c.3611+54_3611+58delinsAACAG (MSH6)	NP_001268421.1:n.3611+54_3611+58delinsAACAG
NM_001281493.2:c.3095+54_3095+58delinsAACAG (MSH6)	NP_001268422.1:n.3095+54_3095+58delinsAACAG
NM_001281494.2:c.3095+54_3095+58delinsAACAG (MSH6)	NP_001268423.1:n.3095+54_3095+58delinsAACAG