Canonical Allele Identifier: CA1139532235

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799722_47799723insCC , CM000664.2:g.47799722_47799723insCC	GRCh38
NC_000002.11:g.48026861_48026862insCC , CM000664.1:g.48026861_48026862insCC	GRCh37
NC_000002.10:g.47880365_47880366insCC	NCBI36
NG_007111.1:g.21576_21577insCC , LRG_219:g.21576_21577insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1442_1443insCC (MSH6)	ENSP00000406248.2:p.Phe483AspfsTer5
ENST00000420813.6:c.1442_1443insCC (MSH6)	ENSP00000390382.2:p.Phe483AspfsTer5
ENST00000455383.6:c.1442_1443insCC (MSH6)	ENSP00000397484.2:p.Phe483AspfsTer5
ENST00000700004.2:c.1739_1740insCC (MSH6)	ENSP00000514752.2:p.Phe582AspfsTer5
ENST00000699999.1:n.1823_1824insCC (MSH6)
ENST00000700000.1:c.1606+133_1606+134insCC (MSH6)	ENSP00000514749.1:n.1606+133_1606+134insCC
ENST00000700002.1:c.1745_1746insCC (MSH6)	ENSP00000514750.1:p.Phe584AspfsTer5
ENST00000700003.1:c.627+3659_627+3660insCC (MSH6)	ENSP00000514751.1:n.627+3659_627+3660insCC
ENST00000700004.1:c.896_897insCC (MSH6)	ENSP00000514752.1:p.Phe301AspfsTer5
ENST00000234420.11:c.1739_1740insCC (MSH6) MANE Select	ENSP00000234420.5:p.Phe582AspfsTer5
ENST00000540021.6:c.1349_1350insCC (MSH6)	ENSP00000446475.1:p.Phe452AspfsTer5
ENST00000652107.1:c.1442_1443insCC (MSH6)	ENSP00000498629.1:p.Phe483AspfsTer5
ENST00000673637.1:c.1442_1443insCC (MSH6)	ENSP00000501310.1:p.Phe483AspfsTer5
ENST00000234420.9:c.1739_1740insCC (MSH6)	ENSP00000234420.4:p.Phe582AspfsTer5
ENST00000405808.5:c.169+8473_169+8474insGG (FBXO11)	ENSP00000385127.1:n.169+8473_169+8474insGG
ENST00000434234.5:c.*124+8272_*124+8273insGG (FBXO11)	ENSP00000402692.1:n.*124+8272_*124+8273insGG
ENST00000445503.5:c.*1086_*1087insCC (MSH6)	ENSP00000405294.1:n.*1086_*1087insCC
ENST00000538136.1:c.833_834insCC (MSH6)	ENSP00000438580.1:p.Phe280AspfsTer5
ENST00000540021.5:c.1349_1350insCC (MSH6)	ENSP00000446475.1:p.Phe452AspfsTer5
ENST00000614496.4:c.833_834insCC (MSH6)	ENSP00000477844.1:p.Phe280AspfsTer5
ENST00000616033.4:c.1736_1737insCC (MSH6)	ENSP00000480261.1:p.Phe581AspfsTer5
ENST00000622629.4:c.-1358_-1357insCC (MSH6)	ENSP00000482078.1:n.-1358_-1357insCC
NM_000179.2:c.1739_1740insCC , LRG_219t1:c.1739_1740insCC (MSH6)	NP_000170.1:p.Phe582AspfsTer5
NM_001281492.1:c.1349_1350insCC (MSH6)	NP_001268421.1:p.Phe452AspfsTer5
NM_001281493.1:c.833_834insCC (MSH6)	NP_001268422.1:p.Phe280AspfsTer5
NM_001281494.1:c.833_834insCC (MSH6)	NP_001268423.1:p.Phe280AspfsTer5
XM_005264271.1:c.1442_1443insCC (MSH6)	XP_005264328.1:p.Phe483AspfsTer5
XM_011532798.1:c.1556_1557insCC (MSH6)	XP_011531100.1:p.Phe521AspfsTer5
XM_011532799.1:c.1442_1443insCC (MSH6)	XP_011531101.1:p.Phe483AspfsTer5
XM_011532800.1:c.1442_1443insCC (MSH6)	XP_011531102.1:p.Phe483AspfsTer5
XM_024452819.1:c.1739_1740insCC (MSH6)	XP_024308587.1:p.Phe582AspfsTer5
XM_024452820.1:c.1556_1557insCC (MSH6)	XP_024308588.1:p.Phe521AspfsTer5
XM_024452821.1:c.1442_1443insCC (MSH6)	XP_024308589.1:p.Phe483AspfsTer5
XM_024452822.1:c.833_834insCC (MSH6)	XP_024308590.1:p.Phe280AspfsTer5
NM_000179.3:c.1739_1740insCC (MSH6) MANE Select	NP_000170.1:p.Phe582AspfsTer5
NM_001281492.2:c.1349_1350insCC (MSH6)	NP_001268421.1:p.Phe452AspfsTer5
NM_001281493.2:c.833_834insCC (MSH6)	NP_001268422.1:p.Phe280AspfsTer5
NM_001281494.2:c.833_834insCC (MSH6)	NP_001268423.1:p.Phe280AspfsTer5