Canonical Allele Identifier: CA008601

Gene: MSH6 FBXO11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799404_47799405dup , CM000664.2:g.47799404_47799405dup	GRCh38
NC_000002.11:g.48026543_48026544dup , CM000664.1:g.48026543_48026544dup	GRCh37
NC_000002.10:g.47880047_47880048dup	NCBI36
NG_007111.1:g.21258_21259dup , LRG_219:g.21258_21259dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1124_1125dup (MSH6)	ENSP00000406248.2:p.Gln376CysfsTer7
ENST00000420813.6:c.1124_1125dup (MSH6)	ENSP00000390382.2:p.Gln376CysfsTer7
ENST00000455383.6:c.1124_1125dup (MSH6)	ENSP00000397484.2:p.Gln376CysfsTer7
ENST00000700004.2:c.1421_1422dup (MSH6)	ENSP00000514752.2:p.Gln475CysfsTer7
ENST00000699999.1:n.1505_1506dup (MSH6)
ENST00000700000.1:c.1421_1422dup (MSH6)	ENSP00000514749.1:p.Gln475CysfsTer7
ENST00000700002.1:c.1427_1428dup (MSH6)	ENSP00000514750.1:p.Gln477CysfsTer7
ENST00000700003.1:c.627+3341_627+3342dup (MSH6)	ENSP00000514751.1:n.627+3341_627+3342dup
ENST00000700004.1:c.578_579dup (MSH6)	ENSP00000514752.1:p.Gln194CysfsTer7
ENST00000234420.11:c.1421_1422dup (MSH6) MANE Select	ENSP00000234420.5:p.Gln475CysfsTer7
ENST00000540021.6:c.1031_1032dup (MSH6)	ENSP00000446475.1:p.Gln345CysfsTer7
ENST00000652107.1:c.1124_1125dup (MSH6)	ENSP00000498629.1:p.Gln376CysfsTer7
ENST00000673637.1:c.1124_1125dup (MSH6)	ENSP00000501310.1:p.Gln376CysfsTer7
ENST00000234420.9:c.1421_1422dup (MSH6)	ENSP00000234420.4:p.Gln475CysfsTer7
ENST00000405808.5:c.169+8791_169+8792dup (FBXO11)	ENSP00000385127.1:n.169+8791_169+8792dup
ENST00000434234.5:c.*124+8590_*124+8591dup (FBXO11)	ENSP00000402692.1:n.*124+8590_*124+8591dup
ENST00000445503.5:c.*768_*769dup (MSH6)	ENSP00000405294.1:n.*768_*769dup
ENST00000538136.1:c.515_516dup (MSH6)	ENSP00000438580.1:p.Gln173CysfsTer7
ENST00000540021.5:c.1031_1032dup (MSH6)	ENSP00000446475.1:p.Gln345CysfsTer7
ENST00000614496.4:c.515_516dup (MSH6)	ENSP00000477844.1:p.Gln173CysfsTer7
ENST00000616033.4:c.1418_1419dup (MSH6)	ENSP00000480261.1:p.Gln474CysfsTer7
ENST00000622629.4:c.-1676_-1675dup (MSH6)	ENSP00000482078.1:n.-1676_-1675dup
NM_000179.2:c.1421_1422dup , LRG_219t1:c.1421_1422dup (MSH6)	NP_000170.1:p.Gln475CysfsTer7
NM_001281492.1:c.1031_1032dup (MSH6)	NP_001268421.1:p.Gln345CysfsTer7
NM_001281493.1:c.515_516dup (MSH6)	NP_001268422.1:p.Gln173CysfsTer7
NM_001281494.1:c.515_516dup (MSH6)	NP_001268423.1:p.Gln173CysfsTer7
XM_005264271.1:c.1124_1125dup (MSH6)	XP_005264328.1:p.Gln376CysfsTer7
XM_011532798.1:c.1238_1239dup (MSH6)	XP_011531100.1:p.Gln414CysfsTer7
XM_011532799.1:c.1124_1125dup (MSH6)	XP_011531101.1:p.Gln376CysfsTer7
XM_011532800.1:c.1124_1125dup (MSH6)	XP_011531102.1:p.Gln376CysfsTer7
XM_024452819.1:c.1421_1422dup (MSH6)	XP_024308587.1:p.Gln475CysfsTer7
XM_024452820.1:c.1238_1239dup (MSH6)	XP_024308588.1:p.Gln414CysfsTer7
XM_024452821.1:c.1124_1125dup (MSH6)	XP_024308589.1:p.Gln376CysfsTer7
XM_024452822.1:c.515_516dup (MSH6)	XP_024308590.1:p.Gln173CysfsTer7
NM_000179.3:c.1421_1422dup (MSH6) MANE Select	NP_000170.1:p.Gln475CysfsTer7
NM_001281492.2:c.1031_1032dup (MSH6)	NP_001268421.1:p.Gln345CysfsTer7
NM_001281493.2:c.515_516dup (MSH6)	NP_001268422.1:p.Gln173CysfsTer7
NM_001281494.2:c.515_516dup (MSH6)	NP_001268423.1:p.Gln173CysfsTer7