Canonical Allele Identifier: CA2496054308

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806590_47806603delinsCAAAAGGGACATAG , CM000664.2:g.47806590_47806603delinsCAAAAGGGACATAG	GRCh38
NC_000002.11:g.48033729_48033742delinsCAAAAGGGACATAG , CM000664.1:g.48033729_48033742delinsCAAAAGGGACATAG	GRCh37
NC_000002.10:g.47887233_47887246delinsCAAAAGGGACATAG	NCBI36
NG_007111.1:g.28444_28457delinsCAAAAGGGACATAG , LRG_219:g.28444_28457delinsCAAAAGGGACATAG
NG_008397.1:g.104073_104086delinsCTATGTCCCTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	ENSP00000406248.2:p.Gln1215=
ENST00000420813.6:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	ENSP00000390382.2:p.Gln1215=
ENST00000455383.6:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	ENSP00000397484.2:p.Gln1215=
ENST00000700004.2:c.3556_3569delinsCAAAAGGGACATAG (MSH6)	ENSP00000514752.2:p.Gln1186=
ENST00000699999.1:n.4614_4627delinsCAAAAGGGACATAG (MSH6)
ENST00000700000.1:c.2374_2387delinsCAAAAGGGACATAG (MSH6)	ENSP00000514749.1:p.Gln792=
ENST00000700002.1:c.3946_3959delinsCAAAAGGGACATAG (MSH6)	ENSP00000514750.1:p.Gln1316=
ENST00000700003.1:c.1395_1408delinsCAAAAGGGACATAG (MSH6)	ENSP00000514751.1:n.1395_1408delinsCAAAAGGGACATAG
ENST00000700004.1:c.2713_2726delinsCAAAAGGGACATAG (MSH6)	ENSP00000514752.1:p.Gln905=
ENST00000700005.1:n.2791_2804delinsCAAAAGGGACATAG (MSH6)
ENST00000700006.1:n.5098_5111delinsCAAAAGGGACATAG (MSH6)
ENST00000700007.1:n.2535_2548delinsCAAAAGGGACATAG (MSH6)
ENST00000700008.1:n.2202_2215delinsCAAAAGGGACATAG (MSH6)
ENST00000700009.1:n.2604_2617delinsCAAAAGGGACATAG (MSH6)
ENST00000700010.1:n.1349_1362delinsCAAAAGGGACATAG (MSH6)
ENST00000700011.1:n.3234_3247delinsCAAAAGGGACATAG (MSH6)
ENST00000682451.1:n.4145_4158delinsCTATGTCCCTTTTG (FBXO11)
ENST00000684712.1:n.4407_4420delinsCTATGTCCCTTTTG (FBXO11)
ENST00000234420.11:c.3940_3953delinsCAAAAGGGACATAG (MSH6) MANE Select	ENSP00000234420.5:p.Gln1314=
ENST00000540021.6:c.3550_3563delinsCAAAAGGGACATAG (MSH6)	ENSP00000446475.1:p.Gln1184=
ENST00000652107.1:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	ENSP00000498629.1:p.Gln1215=
ENST00000673637.1:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	ENSP00000501310.1:p.Gln1215=
ENST00000234420.9:c.3940_3953delinsCAAAAGGGACATAG (MSH6)	ENSP00000234420.4:p.Gln1314=
ENST00000405808.5:c.169+1592_169+1605delinsCTATGTCCCTTTTG (FBXO11)	ENSP00000385127.1:n.169+1592_169+1605delinsCTATGTCCCTTTTG
ENST00000434234.5:c.*124+1391_*124+1404delinsCTATGTCCCTTTTG (FBXO11)	ENSP00000402692.1:n.*124+1391_*124+1404delinsCTATGTCCCTTTTG
ENST00000445503.5:c.*3287_*3300delinsCAAAAGGGACATAG (MSH6)	ENSP00000405294.1:n.*3287_*3300delinsCAAAAGGGACATAG
ENST00000538136.1:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	ENSP00000438580.1:p.Gln1012=
ENST00000540021.5:c.3550_3563delinsCAAAAGGGACATAG (MSH6)	ENSP00000446475.1:p.Gln1184=
ENST00000614496.4:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	ENSP00000477844.1:p.Gln1012=
ENST00000622629.4:c.841_854delinsCAAAAGGGACATAG (MSH6)	ENSP00000482078.1:p.Gln281=
NM_000179.2:c.3940_3953delinsCAAAAGGGACATAG , LRG_219t1:c.3940_3953delinsCAAAAGGGACATAG (MSH6)	NP_000170.1:p.Gln1314=
NM_001281492.1:c.3550_3563delinsCAAAAGGGACATAG (MSH6)	NP_001268421.1:p.Gln1184=
NM_001281493.1:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	NP_001268422.1:p.Gln1012=
NM_001281494.1:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	NP_001268423.1:p.Gln1012=
XM_005264271.1:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	XP_005264328.1:p.Gln1215=
XM_011532798.1:c.3757_3770delinsCAAAAGGGACATAG (MSH6)	XP_011531100.1:p.Gln1253=
XM_011532799.1:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	XP_011531101.1:p.Gln1215=
XM_011532800.1:c.3643_3656delinsCAAAAGGGACATAG (MSH6)	XP_011531102.1:p.Gln1215=
XM_024452819.1:c.4033_4046delinsCAAAAGGGACATAG (MSH6)	XP_024308587.1:p.Gln1345=
XM_024452820.1:c.3850_3863delinsCAAAAGGGACATAG (MSH6)	XP_024308588.1:p.Gln1284=
XM_024452821.1:c.3736_3749delinsCAAAAGGGACATAG (MSH6)	XP_024308589.1:p.Gln1246=
XM_024452822.1:c.3127_3140delinsCAAAAGGGACATAG (MSH6)	XP_024308590.1:p.Gln1043=
NM_000179.3:c.3940_3953delinsCAAAAGGGACATAG (MSH6) MANE Select	NP_000170.1:p.Gln1314=
NM_001281492.2:c.3550_3563delinsCAAAAGGGACATAG (MSH6)	NP_001268421.1:p.Gln1184=
NM_001281493.2:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	NP_001268422.1:p.Gln1012=
NM_001281494.2:c.3034_3047delinsCAAAAGGGACATAG (MSH6)	NP_001268423.1:p.Gln1012=