Canonical Allele Identifier: CA2496054061

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806455_47806468delinsTGCATGGTAGAAAA , CM000664.2:g.47806455_47806468delinsTGCATGGTAGAAAA	GRCh38
NC_000002.11:g.48033594_48033607delinsTGCATGGTAGAAAA , CM000664.1:g.48033594_48033607delinsTGCATGGTAGAAAA	GRCh37
NC_000002.10:g.47887098_47887111delinsTGCATGGTAGAAAA	NCBI36
NG_007111.1:g.28309_28322delinsTGCATGGTAGAAAA , LRG_219:g.28309_28322delinsTGCATGGTAGAAAA
NG_008397.1:g.104208_104221delinsTTTTCTACCATGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	ENSP00000406248.2:p.Cys1170=
ENST00000420813.6:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	ENSP00000390382.2:p.Cys1170=
ENST00000455383.6:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	ENSP00000397484.2:p.Cys1170=
ENST00000700004.2:c.3421_3434delinsTGCATGGTAGAAAA (MSH6)	ENSP00000514752.2:p.Cys1141=
ENST00000699999.1:n.4479_4492delinsTGCATGGTAGAAAA (MSH6)
ENST00000700000.1:c.2239_2252delinsTGCATGGTAGAAAA (MSH6)	ENSP00000514749.1:p.Cys747=
ENST00000700002.1:c.3811_3824delinsTGCATGGTAGAAAA (MSH6)	ENSP00000514750.1:p.Cys1271=
ENST00000700003.1:c.1260_1273delinsTGCATGGTAGAAAA (MSH6)	ENSP00000514751.1:n.1260_1273delinsTGCATGGTAGAAAA
ENST00000700004.1:c.2578_2591delinsTGCATGGTAGAAAA (MSH6)	ENSP00000514752.1:p.Cys860=
ENST00000700005.1:n.2656_2669delinsTGCATGGTAGAAAA (MSH6)
ENST00000700006.1:n.4963_4976delinsTGCATGGTAGAAAA (MSH6)
ENST00000700007.1:n.2400_2413delinsTGCATGGTAGAAAA (MSH6)
ENST00000700008.1:n.2067_2080delinsTGCATGGTAGAAAA (MSH6)
ENST00000700009.1:n.2469_2482delinsTGCATGGTAGAAAA (MSH6)
ENST00000700010.1:n.1214_1227delinsTGCATGGTAGAAAA (MSH6)
ENST00000700011.1:n.3099_3112delinsTGCATGGTAGAAAA (MSH6)
ENST00000682451.1:n.4280_4293delinsTTTTCTACCATGCA (FBXO11)
ENST00000684712.1:n.4542_4555delinsTTTTCTACCATGCA (FBXO11)
ENST00000234420.11:c.3805_3818delinsTGCATGGTAGAAAA (MSH6) MANE Select	ENSP00000234420.5:p.Cys1269=
ENST00000540021.6:c.3415_3428delinsTGCATGGTAGAAAA (MSH6)	ENSP00000446475.1:p.Cys1139=
ENST00000652107.1:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	ENSP00000498629.1:p.Cys1170=
ENST00000673637.1:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	ENSP00000501310.1:p.Cys1170=
ENST00000234420.9:c.3805_3818delinsTGCATGGTAGAAAA (MSH6)	ENSP00000234420.4:p.Cys1269=
ENST00000405808.5:c.169+1727_169+1740delinsTTTTCTACCATGCA (FBXO11)	ENSP00000385127.1:n.169+1727_169+1740delinsTTTTCTACCATGCA
ENST00000434234.5:c.*124+1526_*124+1539delinsTTTTCTACCATGCA (FBXO11)	ENSP00000402692.1:n.*124+1526_*124+1539delinsTTTTCTACCATGCA
ENST00000445503.5:c.*3152_*3165delinsTGCATGGTAGAAAA (MSH6)	ENSP00000405294.1:n.*3152_*3165delinsTGCATGGTAGAAAA
ENST00000538136.1:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	ENSP00000438580.1:p.Cys967=
ENST00000540021.5:c.3415_3428delinsTGCATGGTAGAAAA (MSH6)	ENSP00000446475.1:p.Cys1139=
ENST00000614496.4:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	ENSP00000477844.1:p.Cys967=
ENST00000622629.4:c.706_719delinsTGCATGGTAGAAAA (MSH6)	ENSP00000482078.1:p.Cys236=
NM_000179.2:c.3805_3818delinsTGCATGGTAGAAAA , LRG_219t1:c.3805_3818delinsTGCATGGTAGAAAA (MSH6)	NP_000170.1:p.Cys1269=
NM_001281492.1:c.3415_3428delinsTGCATGGTAGAAAA (MSH6)	NP_001268421.1:p.Cys1139=
NM_001281493.1:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	NP_001268422.1:p.Cys967=
NM_001281494.1:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	NP_001268423.1:p.Cys967=
XM_005264271.1:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	XP_005264328.1:p.Cys1170=
XM_011532798.1:c.3622_3635delinsTGCATGGTAGAAAA (MSH6)	XP_011531100.1:p.Cys1208=
XM_011532799.1:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	XP_011531101.1:p.Cys1170=
XM_011532800.1:c.3508_3521delinsTGCATGGTAGAAAA (MSH6)	XP_011531102.1:p.Cys1170=
XM_024452819.1:c.3898_3911delinsTGCATGGTAGAAAA (MSH6)	XP_024308587.1:p.Cys1300=
XM_024452820.1:c.3715_3728delinsTGCATGGTAGAAAA (MSH6)	XP_024308588.1:p.Cys1239=
XM_024452821.1:c.3601_3614delinsTGCATGGTAGAAAA (MSH6)	XP_024308589.1:p.Cys1201=
XM_024452822.1:c.2992_3005delinsTGCATGGTAGAAAA (MSH6)	XP_024308590.1:p.Cys998=
NM_000179.3:c.3805_3818delinsTGCATGGTAGAAAA (MSH6) MANE Select	NP_000170.1:p.Cys1269=
NM_001281492.2:c.3415_3428delinsTGCATGGTAGAAAA (MSH6)	NP_001268421.1:p.Cys1139=
NM_001281493.2:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	NP_001268422.1:p.Cys967=
NM_001281494.2:c.2899_2912delinsTGCATGGTAGAAAA (MSH6)	NP_001268423.1:p.Cys967=