Canonical Allele Identifier: CA2580068100

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1797324
• ClinVar RCV Id: RCV002437949 ; RCV003759754

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800875dup , CM000664.2:g.47800875dup	GRCh38
NC_000002.11:g.48028014dup , CM000664.1:g.48028014dup	GRCh37
NC_000002.10:g.47881518dup	NCBI36
NG_007111.1:g.22729dup , LRG_219:g.22729dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2595dup (MSH6)	ENSP00000406248.2:p.Arg866Ter
ENST00000420813.6:c.2595dup (MSH6)	ENSP00000390382.2:p.Arg866Ter
ENST00000455383.6:c.2595dup (MSH6)	ENSP00000397484.2:p.Arg866Ter
ENST00000700004.2:c.2892dup (MSH6)	ENSP00000514752.2:p.Arg965Ter
ENST00000699999.1:n.2976dup (MSH6)
ENST00000700000.1:c.1606+1286dup (MSH6)	ENSP00000514749.1:n.1606+1286dup
ENST00000700002.1:c.2898dup (MSH6)	ENSP00000514750.1:p.Arg967Ter
ENST00000700003.1:c.628-2545dup (MSH6)	ENSP00000514751.1:n.628-2545dup
ENST00000700004.1:c.2049dup (MSH6)	ENSP00000514752.1:p.Arg684Ter
ENST00000234420.11:c.2892dup (MSH6) MANE Select	ENSP00000234420.5:p.Arg965Ter
ENST00000540021.6:c.2502dup (MSH6)	ENSP00000446475.1:p.Arg835Ter
ENST00000652107.1:c.2595dup (MSH6)	ENSP00000498629.1:p.Arg866Ter
ENST00000673637.1:c.2595dup (MSH6)	ENSP00000501310.1:p.Arg866Ter
ENST00000234420.9:c.2892dup (MSH6)	ENSP00000234420.4:p.Arg965Ter
ENST00000405808.5:c.169+7320dup (FBXO11)	ENSP00000385127.1:n.169+7320dup
ENST00000434234.5:c.*124+7119dup (FBXO11)	ENSP00000402692.1:n.*124+7119dup
ENST00000445503.5:c.*2239dup (MSH6)	ENSP00000405294.1:n.*2239dup
ENST00000538136.1:c.1986dup (MSH6)	ENSP00000438580.1:p.Arg663Ter
ENST00000540021.5:c.2502dup (MSH6)	ENSP00000446475.1:p.Arg835Ter
ENST00000614496.4:c.1986dup (MSH6)	ENSP00000477844.1:p.Arg663Ter
ENST00000616033.4:c.2889dup (MSH6)	ENSP00000480261.1:p.Arg964Ter
ENST00000622629.4:c.-205dup (MSH6)	ENSP00000482078.1:n.-205dup
NM_000179.2:c.2892dup , LRG_219t1:c.2892dup (MSH6)	NP_000170.1:p.Arg965Ter
NM_001281492.1:c.2502dup (MSH6)	NP_001268421.1:p.Arg835Ter
NM_001281493.1:c.1986dup (MSH6)	NP_001268422.1:p.Arg663Ter
NM_001281494.1:c.1986dup (MSH6)	NP_001268423.1:p.Arg663Ter
XM_005264271.1:c.2595dup (MSH6)	XP_005264328.1:p.Arg866Ter
XM_011532798.1:c.2709dup (MSH6)	XP_011531100.1:p.Arg904Ter
XM_011532799.1:c.2595dup (MSH6)	XP_011531101.1:p.Arg866Ter
XM_011532800.1:c.2595dup (MSH6)	XP_011531102.1:p.Arg866Ter
XM_024452819.1:c.2892dup (MSH6)	XP_024308587.1:p.Arg965Ter
XM_024452820.1:c.2709dup (MSH6)	XP_024308588.1:p.Arg904Ter
XM_024452821.1:c.2595dup (MSH6)	XP_024308589.1:p.Arg866Ter
XM_024452822.1:c.1986dup (MSH6)	XP_024308590.1:p.Arg663Ter
NM_000179.3:c.2892dup (MSH6) MANE Select	NP_000170.1:p.Arg965Ter
NM_001281492.2:c.2502dup (MSH6)	NP_001268421.1:p.Arg835Ter
NM_001281493.2:c.1986dup (MSH6)	NP_001268422.1:p.Arg663Ter
NM_001281494.2:c.1986dup (MSH6)	NP_001268423.1:p.Arg663Ter