Canonical Allele Identifier: CA2496052971

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805027_47805038delinsGGTGAGTTTTTT , CM000664.2:g.47805027_47805038delinsGGTGAGTTTTTT	GRCh38
NC_000002.11:g.48032166_48032177delinsGGTGAGTTTTTT , CM000664.1:g.48032166_48032177delinsGGTGAGTTTTTT	GRCh37
NC_000002.10:g.47885670_47885681delinsGGTGAGTTTTTT	NCBI36
NG_007111.1:g.26881_26892delinsGGTGAGTTTTTT , LRG_219:g.26881_26892delinsGGTGAGTTTTTT
NG_008397.1:g.105638_105649delinsAAAAAACTCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
ENST00000420813.6:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
ENST00000455383.6:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700004.2:c.3173-591_3173-580delinsGGTGAGTTTTTT (MSH6)	ENSP00000514752.2:n.3173-591_3173-580delinsGGTGAGTTTTTT
ENST00000699999.1:n.3640_3651delinsGGTGAGTTTTTT (MSH6)
ENST00000700000.1:c.1990_1990+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700002.1:c.3562_3562+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700003.1:c.1011_1011+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700004.1:c.2330-591_2330-580delinsGGTGAGTTTTTT (MSH6)	ENSP00000514752.1:n.2330-591_2330-580delinsGGTGAGTTTTTT
ENST00000700005.1:n.2407_2407+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700006.1:n.3628_3639delinsGGTGAGTTTTTT (MSH6)
ENST00000700007.1:n.1561_1572delinsGGTGAGTTTTTT (MSH6)
ENST00000700008.1:n.1135_1146delinsGGTGAGTTTTTT (MSH6)
ENST00000700009.1:n.1134_1145delinsGGTGAGTTTTTT (MSH6)
ENST00000700010.1:n.965_965+11delinsGGTGAGTTTTTT (MSH6)
ENST00000700011.1:n.2260_2271delinsGGTGAGTTTTTT (MSH6)
ENST00000234420.11:c.3556_3556+11delinsGGTGAGTTTTTT (MSH6)
ENST00000540021.6:c.3166_3166+11delinsGGTGAGTTTTTT (MSH6)
ENST00000652107.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
ENST00000673637.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
ENST00000234420.9:c.3556_3556+11delinsGGTGAGTTTTTT (MSH6)
ENST00000405808.5:c.169+3157_169+3168delinsAAAAAACTCACC (FBXO11)	ENSP00000385127.1:n.169+3157_169+3168delinsAAAAAACTCACC
ENST00000434234.5:c.*124+2956_*124+2967delinsAAAAAACTCACC (FBXO11)	ENSP00000402692.1:n.*124+2956_*124+2967delinsAAAAAACTCACC
ENST00000445503.5:c.*2903_*2903+11delinsGGTGAGTTTTTT (MSH6)
ENST00000538136.1:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
ENST00000540021.5:c.3166_3166+11delinsGGTGAGTTTTTT (MSH6)
ENST00000614496.4:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
ENST00000622629.4:c.460_460+11delinsGGTGAGTTTTTT (MSH6)
NM_000179.2:c.3556_3556+11delinsGGTGAGTTTTTT , LRG_219t1:c.3556_3556+11delinsGGTGAGTTTTTT (MSH6)
NM_001281492.1:c.3166_3166+11delinsGGTGAGTTTTTT (MSH6)
NM_001281493.1:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
NM_001281494.1:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
XM_005264271.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
XM_011532798.1:c.3373_3373+11delinsGGTGAGTTTTTT (MSH6)
XM_011532799.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
XM_011532800.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
XM_024452819.1:c.3556_3556+11delinsGGTGAGTTTTTT (MSH6)
XM_024452820.1:c.3373_3373+11delinsGGTGAGTTTTTT (MSH6)
XM_024452821.1:c.3259_3259+11delinsGGTGAGTTTTTT (MSH6)
XM_024452822.1:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
NM_000179.3:c.3556_3556+11delinsGGTGAGTTTTTT (MSH6)
NM_001281492.2:c.3166_3166+11delinsGGTGAGTTTTTT (MSH6)
NM_001281493.2:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)
NM_001281494.2:c.2650_2650+11delinsGGTGAGTTTTTT (MSH6)