Canonical Allele Identifier: CA2496054234

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806353_47806354delinsCA , CM000664.2:g.47806353_47806354delinsCA	GRCh38
NC_000002.11:g.48033492_48033493delinsCA , CM000664.1:g.48033492_48033493delinsCA	GRCh37
NC_000002.10:g.47886996_47886997delinsCA	NCBI36
NG_007111.1:g.28207_28208delinsCA , LRG_219:g.28207_28208delinsCA
NG_008397.1:g.104322_104323delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3499_3500delinsCA (MSH6)	ENSP00000406248.2:p.His1167=
ENST00000420813.6:c.3499_3500delinsCA (MSH6)	ENSP00000390382.2:p.His1167=
ENST00000455383.6:c.3499_3500delinsCA (MSH6)	ENSP00000397484.2:p.His1167=
ENST00000700004.2:c.3412_3413delinsCA (MSH6)	ENSP00000514752.2:p.His1138=
ENST00000699999.1:n.4470_4471delinsCA (MSH6)
ENST00000700000.1:c.2230_2231delinsCA (MSH6)	ENSP00000514749.1:p.His744=
ENST00000700002.1:c.3802_3803delinsCA (MSH6)	ENSP00000514750.1:p.His1268=
ENST00000700003.1:c.1251_1252delinsCA (MSH6)	ENSP00000514751.1:n.1251_1252delinsCA
ENST00000700004.1:c.2569_2570delinsCA (MSH6)	ENSP00000514752.1:p.His857=
ENST00000700005.1:n.2647_2648delinsCA (MSH6)
ENST00000700006.1:n.4954_4955delinsCA (MSH6)
ENST00000700007.1:n.2391_2392delinsCA (MSH6)
ENST00000700008.1:n.1965_1966delinsCA (MSH6)
ENST00000700009.1:n.2460_2461delinsCA (MSH6)
ENST00000700010.1:n.1205_1206delinsCA (MSH6)
ENST00000700011.1:n.3090_3091delinsCA (MSH6)
ENST00000682451.1:n.4394_4395delinsTG (FBXO11)
ENST00000684712.1:n.4656_4657delinsTG (FBXO11)
ENST00000234420.11:c.3796_3797delinsCA (MSH6) MANE Select	ENSP00000234420.5:p.His1266=
ENST00000540021.6:c.3406_3407delinsCA (MSH6)	ENSP00000446475.1:p.His1136=
ENST00000652107.1:c.3499_3500delinsCA (MSH6)	ENSP00000498629.1:p.His1167=
ENST00000673637.1:c.3499_3500delinsCA (MSH6)	ENSP00000501310.1:p.His1167=
ENST00000234420.9:c.3796_3797delinsCA (MSH6)	ENSP00000234420.4:p.His1266=
ENST00000405808.5:c.169+1841_169+1842delinsTG (FBXO11)	ENSP00000385127.1:n.169+1841_169+1842delinsTG
ENST00000434234.5:c.*124+1640_*124+1641delinsTG (FBXO11)	ENSP00000402692.1:n.*124+1640_*124+1641delinsTG
ENST00000445503.5:c.*3143_*3144delinsCA (MSH6)	ENSP00000405294.1:n.*3143_*3144delinsCA
ENST00000538136.1:c.2890_2891delinsCA (MSH6)	ENSP00000438580.1:p.His964=
ENST00000540021.5:c.3406_3407delinsCA (MSH6)	ENSP00000446475.1:p.His1136=
ENST00000614496.4:c.2890_2891delinsCA (MSH6)	ENSP00000477844.1:p.His964=
ENST00000622629.4:c.697_698delinsCA (MSH6)	ENSP00000482078.1:p.His233=
NM_000179.2:c.3796_3797delinsCA , LRG_219t1:c.3796_3797delinsCA (MSH6)	NP_000170.1:p.His1266=
NM_001281492.1:c.3406_3407delinsCA (MSH6)	NP_001268421.1:p.His1136=
NM_001281493.1:c.2890_2891delinsCA (MSH6)	NP_001268422.1:p.His964=
NM_001281494.1:c.2890_2891delinsCA (MSH6)	NP_001268423.1:p.His964=
XM_005264271.1:c.3499_3500delinsCA (MSH6)	XP_005264328.1:p.His1167=
XM_011532798.1:c.3613_3614delinsCA (MSH6)	XP_011531100.1:p.His1205=
XM_011532799.1:c.3499_3500delinsCA (MSH6)	XP_011531101.1:p.His1167=
XM_011532800.1:c.3499_3500delinsCA (MSH6)	XP_011531102.1:p.His1167=
XM_024452819.1:c.3796_3797delinsCA (MSH6)	XP_024308587.1:p.His1266=
XM_024452820.1:c.3613_3614delinsCA (MSH6)	XP_024308588.1:p.His1205=
XM_024452821.1:c.3499_3500delinsCA (MSH6)	XP_024308589.1:p.His1167=
XM_024452822.1:c.2890_2891delinsCA (MSH6)	XP_024308590.1:p.His964=
NM_000179.3:c.3796_3797delinsCA (MSH6) MANE Select	NP_000170.1:p.His1266=
NM_001281492.2:c.3406_3407delinsCA (MSH6)	NP_001268421.1:p.His1136=
NM_001281493.2:c.2890_2891delinsCA (MSH6)	NP_001268422.1:p.His964=
NM_001281494.2:c.2890_2891delinsCA (MSH6)	NP_001268423.1:p.His964=