Canonical Allele Identifier: CA2496052957

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805016_47805019delinsGAAT , CM000664.2:g.47805016_47805019delinsGAAT	GRCh38
NC_000002.11:g.48032155_48032158delinsGAAT , CM000664.1:g.48032155_48032158delinsGAAT	GRCh37
NC_000002.10:g.47885659_47885662delinsGAAT	NCBI36
NG_007111.1:g.26870_26873delinsGAAT , LRG_219:g.26870_26873delinsGAAT
NG_008397.1:g.105657_105660delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3248_3251delinsGAAT (MSH6)	ENSP00000406248.2:p.Arg1083=
ENST00000420813.6:c.3248_3251delinsGAAT (MSH6)	ENSP00000390382.2:p.Arg1083=
ENST00000455383.6:c.3248_3251delinsGAAT (MSH6)	ENSP00000397484.2:p.Arg1083=
ENST00000700004.2:c.3173-602_3173-599delinsGAAT (MSH6)	ENSP00000514752.2:n.3173-602_3173-599delinsGAAT
ENST00000699999.1:n.3629_3632delinsGAAT (MSH6)
ENST00000700000.1:c.1979_1982delinsGAAT (MSH6)	ENSP00000514749.1:p.Arg660=
ENST00000700002.1:c.3551_3554delinsGAAT (MSH6)	ENSP00000514750.1:p.Arg1184=
ENST00000700003.1:c.1000_1003delinsGAAT (MSH6)	ENSP00000514751.1:n.1000_1003delinsGAAT
ENST00000700004.1:c.2330-602_2330-599delinsGAAT (MSH6)	ENSP00000514752.1:n.2330-602_2330-599delinsGAAT
ENST00000700005.1:n.2396_2399delinsGAAT (MSH6)
ENST00000700006.1:n.3617_3620delinsGAAT (MSH6)
ENST00000700007.1:n.1550_1553delinsGAAT (MSH6)
ENST00000700008.1:n.1124_1127delinsGAAT (MSH6)
ENST00000700009.1:n.1123_1126delinsGAAT (MSH6)
ENST00000700010.1:n.954_957delinsGAAT (MSH6)
ENST00000700011.1:n.2249_2252delinsGAAT (MSH6)
ENST00000234420.11:c.3545_3548delinsGAAT (MSH6) MANE Select	ENSP00000234420.5:p.Arg1182=
ENST00000540021.6:c.3155_3158delinsGAAT (MSH6)	ENSP00000446475.1:p.Arg1052=
ENST00000652107.1:c.3248_3251delinsGAAT (MSH6)	ENSP00000498629.1:p.Arg1083=
ENST00000673637.1:c.3248_3251delinsGAAT (MSH6)	ENSP00000501310.1:p.Arg1083=
ENST00000234420.9:c.3545_3548delinsGAAT (MSH6)	ENSP00000234420.4:p.Arg1182=
ENST00000405808.5:c.169+3176_169+3179delinsATTC (FBXO11)	ENSP00000385127.1:n.169+3176_169+3179delinsATTC
ENST00000434234.5:c.*124+2975_*124+2978delinsATTC (FBXO11)	ENSP00000402692.1:n.*124+2975_*124+2978delinsATTC
ENST00000445503.5:c.*2892_*2895delinsGAAT (MSH6)	ENSP00000405294.1:n.*2892_*2895delinsGAAT
ENST00000538136.1:c.2639_2642delinsGAAT (MSH6)	ENSP00000438580.1:p.Arg880=
ENST00000540021.5:c.3155_3158delinsGAAT (MSH6)	ENSP00000446475.1:p.Arg1052=
ENST00000614496.4:c.2639_2642delinsGAAT (MSH6)	ENSP00000477844.1:p.Arg880=
ENST00000622629.4:c.449_452delinsGAAT (MSH6)	ENSP00000482078.1:p.Arg150=
NM_000179.2:c.3545_3548delinsGAAT , LRG_219t1:c.3545_3548delinsGAAT (MSH6)	NP_000170.1:p.Arg1182=
NM_001281492.1:c.3155_3158delinsGAAT (MSH6)	NP_001268421.1:p.Arg1052=
NM_001281493.1:c.2639_2642delinsGAAT (MSH6)	NP_001268422.1:p.Arg880=
NM_001281494.1:c.2639_2642delinsGAAT (MSH6)	NP_001268423.1:p.Arg880=
XM_005264271.1:c.3248_3251delinsGAAT (MSH6)	XP_005264328.1:p.Arg1083=
XM_011532798.1:c.3362_3365delinsGAAT (MSH6)	XP_011531100.1:p.Arg1121=
XM_011532799.1:c.3248_3251delinsGAAT (MSH6)	XP_011531101.1:p.Arg1083=
XM_011532800.1:c.3248_3251delinsGAAT (MSH6)	XP_011531102.1:p.Arg1083=
XM_024452819.1:c.3545_3548delinsGAAT (MSH6)	XP_024308587.1:p.Arg1182=
XM_024452820.1:c.3362_3365delinsGAAT (MSH6)	XP_024308588.1:p.Arg1121=
XM_024452821.1:c.3248_3251delinsGAAT (MSH6)	XP_024308589.1:p.Arg1083=
XM_024452822.1:c.2639_2642delinsGAAT (MSH6)	XP_024308590.1:p.Arg880=
NM_000179.3:c.3545_3548delinsGAAT (MSH6) MANE Select	NP_000170.1:p.Arg1182=
NM_001281492.2:c.3155_3158delinsGAAT (MSH6)	NP_001268421.1:p.Arg1052=
NM_001281493.2:c.2639_2642delinsGAAT (MSH6)	NP_001268422.1:p.Arg880=
NM_001281494.2:c.2639_2642delinsGAAT (MSH6)	NP_001268423.1:p.Arg880=