Canonical Allele Identifier: CA2845003633

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806861_47806863del , CM000664.2:g.47806861_47806863del	GRCh38
NC_000002.11:g.48034000_48034002del , CM000664.1:g.48034000_48034002del	GRCh37
NC_000002.10:g.47887504_47887506del	NCBI36
NG_007111.1:g.28715_28717del , LRG_219:g.28715_28717del
NG_008397.1:g.103813_103815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.*1_*3del (MSH6)	ENSP00000406248.2:n.*1_*3del
ENST00000420813.6:c.*1_*3del (MSH6)	ENSP00000390382.2:n.*1_*3del
ENST00000455383.6:c.*1_*3del (MSH6)	ENSP00000397484.2:n.*1_*3del
ENST00000700004.2:c.*1_*3del (MSH6)	ENSP00000514752.2:n.*1_*3del
ENST00000699999.1:n.4758_4760del (MSH6)
ENST00000700000.1:c.*1_*3del (MSH6)	ENSP00000514749.1:n.*1_*3del
ENST00000700002.1:c.*1_*3del (MSH6)	ENSP00000514750.1:n.*1_*3del
ENST00000700003.1:c.1539_1541del (MSH6)	ENSP00000514751.1:n.1539_1541del
ENST00000700004.1:c.2857_2859del (MSH6)	ENSP00000514752.1:n.2857_2859del
ENST00000700005.1:n.3062_3064del (MSH6)
ENST00000700007.1:n.2679_2681del (MSH6)
ENST00000700008.1:n.2346_2348del (MSH6)
ENST00000700009.1:n.2748_2750del (MSH6)
ENST00000700010.1:n.1493_1495del (MSH6)
ENST00000700011.1:n.3378_3380del (MSH6)
ENST00000682451.1:n.3885_3887del (FBXO11)
ENST00000684712.1:n.4147_4149del (FBXO11)
ENST00000234420.11:c.*1_*3del (MSH6) MANE Select	ENSP00000234420.5:n.*1_*3del
ENST00000540021.6:c.*1_*3del (MSH6)	ENSP00000446475.1:n.*1_*3del
ENST00000652107.1:c.*1_*3del (MSH6)	ENSP00000498629.1:n.*1_*3del
ENST00000673637.1:c.*1_*3del (MSH6)	ENSP00000501310.1:n.*1_*3del
ENST00000234420.9:c.*1_*3del (MSH6)	ENSP00000234420.4:n.*1_*3del
ENST00000405808.5:c.169+1332_169+1334del (FBXO11)	ENSP00000385127.1:n.169+1332_169+1334del
ENST00000434234.5:c.*124+1131_*124+1133del (FBXO11)	ENSP00000402692.1:n.*124+1131_*124+1133del
ENST00000445503.5:c.*3431_*3433del (MSH6)	ENSP00000405294.1:n.*3431_*3433del
ENST00000465204.5:n.3047_3049del (FBXO11)
ENST00000538136.1:c.*1_*3del (MSH6)	ENSP00000438580.1:n.*1_*3del
ENST00000540021.5:c.*1_*3del (MSH6)	ENSP00000446475.1:n.*1_*3del
ENST00000614496.4:c.*1_*3del (MSH6)	ENSP00000477844.1:n.*1_*3del
ENST00000622629.4:c.*1_*3del (MSH6)	ENSP00000482078.1:n.*1_*3del
NM_000179.2:c.*1_*3del , LRG_219t1:c.*1_*3del (MSH6)	NP_000170.1:n.*1_*3del
NM_001281492.1:c.*1_*3del (MSH6)	NP_001268421.1:n.*1_*3del
NM_001281493.1:c.*1_*3del (MSH6)	NP_001268422.1:n.*1_*3del
NM_001281494.1:c.*1_*3del (MSH6)	NP_001268423.1:n.*1_*3del
XM_005264271.1:c.*1_*3del (MSH6)	XP_005264328.1:n.*1_*3del
XM_011532798.1:c.*1_*3del (MSH6)	XP_011531100.1:n.*1_*3del
XM_011532799.1:c.*1_*3del (MSH6)	XP_011531101.1:n.*1_*3del
XM_011532800.1:c.*1_*3del (MSH6)	XP_011531102.1:n.*1_*3del
XM_024452819.1:c.*1_*3del (MSH6)	XP_024308587.1:n.*1_*3del
XM_024452820.1:c.*1_*3del (MSH6)	XP_024308588.1:n.*1_*3del
XM_024452821.1:c.*1_*3del (MSH6)	XP_024308589.1:n.*1_*3del
XM_024452822.1:c.*1_*3del (MSH6)	XP_024308590.1:n.*1_*3del
NM_000179.3:c.*1_*3del (MSH6) MANE Select	NP_000170.1:n.*1_*3del
NM_001281492.2:c.*1_*3del (MSH6)	NP_001268421.1:n.*1_*3del
NM_001281493.2:c.*1_*3del (MSH6)	NP_001268422.1:n.*1_*3del
NM_001281494.2:c.*1_*3del (MSH6)	NP_001268423.1:n.*1_*3del