Canonical Allele Identifier: CA2658967663

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806298-TCACTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806301_47806306del , CM000664.2:g.47806301_47806306del	GRCh38
NC_000002.11:g.48033440_48033445del , CM000664.1:g.48033440_48033445del	GRCh37
NC_000002.10:g.47886944_47886949del	NCBI36
NG_007111.1:g.28155_28160del , LRG_219:g.28155_28160del
NG_008397.1:g.104372_104377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3447_3452del (MSH6)	ENSP00000406248.2:p.Tyr1150_His1151del
ENST00000420813.6:c.3447_3452del (MSH6)	ENSP00000390382.2:p.Tyr1150_His1151del
ENST00000455383.6:c.3447_3452del (MSH6)	ENSP00000397484.2:p.Tyr1150_His1151del
ENST00000700004.2:c.3360_3365del (MSH6)	ENSP00000514752.2:p.Tyr1121_His1122del
ENST00000699999.1:n.4418_4423del (MSH6)
ENST00000700000.1:c.2178_2183del (MSH6)	ENSP00000514749.1:p.Tyr727_His728del
ENST00000700002.1:c.3750_3755del (MSH6)	ENSP00000514750.1:p.Tyr1251_His1252del
ENST00000700003.1:c.1199_1204del (MSH6)	ENSP00000514751.1:n.1199_1204del
ENST00000700004.1:c.2517_2522del (MSH6)	ENSP00000514752.1:p.Tyr840_His841del
ENST00000700005.1:n.2595_2600del (MSH6)
ENST00000700006.1:n.4902_4907del (MSH6)
ENST00000700007.1:n.2339_2344del (MSH6)
ENST00000700008.1:n.1913_1918del (MSH6)
ENST00000700009.1:n.2408_2413del (MSH6)
ENST00000700010.1:n.1153_1158del (MSH6)
ENST00000700011.1:n.3038_3043del (MSH6)
ENST00000682451.1:n.4444_4449del (FBXO11)
ENST00000684712.1:n.4706_4711del (FBXO11)
ENST00000234420.11:c.3744_3749del (MSH6) MANE Select	ENSP00000234420.5:p.Tyr1249_His1250del
ENST00000540021.6:c.3354_3359del (MSH6)	ENSP00000446475.1:p.Tyr1119_His1120del
ENST00000652107.1:c.3447_3452del (MSH6)	ENSP00000498629.1:p.Tyr1150_His1151del
ENST00000673637.1:c.3447_3452del (MSH6)	ENSP00000501310.1:p.Tyr1150_His1151del
ENST00000234420.9:c.3744_3749del (MSH6)	ENSP00000234420.4:p.Tyr1249_His1250del
ENST00000405808.5:c.169+1891_169+1896del (FBXO11)	ENSP00000385127.1:n.169+1891_169+1896del
ENST00000434234.5:c.*124+1690_*124+1695del (FBXO11)	ENSP00000402692.1:n.*124+1690_*124+1695del
ENST00000445503.5:c.*3091_*3096del (MSH6)	ENSP00000405294.1:n.*3091_*3096del
ENST00000538136.1:c.2838_2843del (MSH6)	ENSP00000438580.1:p.Tyr947_His948del
ENST00000540021.5:c.3354_3359del (MSH6)	ENSP00000446475.1:p.Tyr1119_His1120del
ENST00000614496.4:c.2838_2843del (MSH6)	ENSP00000477844.1:p.Tyr947_His948del
ENST00000622629.4:c.648_653del (MSH6)	ENSP00000482078.1:p.Tyr217_His218del
NM_000179.2:c.3744_3749del , LRG_219t1:c.3744_3749del (MSH6)	NP_000170.1:p.Tyr1249_His1250del
NM_001281492.1:c.3354_3359del (MSH6)	NP_001268421.1:p.Tyr1119_His1120del
NM_001281493.1:c.2838_2843del (MSH6)	NP_001268422.1:p.Tyr947_His948del
NM_001281494.1:c.2838_2843del (MSH6)	NP_001268423.1:p.Tyr947_His948del
XM_005264271.1:c.3447_3452del (MSH6)	XP_005264328.1:p.Tyr1150_His1151del
XM_011532798.1:c.3561_3566del (MSH6)	XP_011531100.1:p.Tyr1188_His1189del
XM_011532799.1:c.3447_3452del (MSH6)	XP_011531101.1:p.Tyr1150_His1151del
XM_011532800.1:c.3447_3452del (MSH6)	XP_011531102.1:p.Tyr1150_His1151del
XM_024452819.1:c.3744_3749del (MSH6)	XP_024308587.1:p.Tyr1249_His1250del
XM_024452820.1:c.3561_3566del (MSH6)	XP_024308588.1:p.Tyr1188_His1189del
XM_024452821.1:c.3447_3452del (MSH6)	XP_024308589.1:p.Tyr1150_His1151del
XM_024452822.1:c.2838_2843del (MSH6)	XP_024308590.1:p.Tyr947_His948del
NM_000179.3:c.3744_3749del (MSH6) MANE Select	NP_000170.1:p.Tyr1249_His1250del
NM_001281492.2:c.3354_3359del (MSH6)	NP_001268421.1:p.Tyr1119_His1120del
NM_001281493.2:c.2838_2843del (MSH6)	NP_001268422.1:p.Tyr947_His948del
NM_001281494.2:c.2838_2843del (MSH6)	NP_001268423.1:p.Tyr947_His948del