Canonical Allele Identifier: CA2580611373

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1790512
• ClinVar RCV Id: RCV002459528

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800371_47800373del , CM000664.2:g.47800371_47800373del	GRCh38
NC_000002.11:g.48027510_48027512del , CM000664.1:g.48027510_48027512del	GRCh37
NC_000002.10:g.47881014_47881016del	NCBI36
NG_007111.1:g.22225_22227del , LRG_219:g.22225_22227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2091_2093del (MSH6)	ENSP00000406248.2:p.Glu697del
ENST00000420813.6:c.2091_2093del (MSH6)	ENSP00000390382.2:p.Glu697del
ENST00000455383.6:c.2091_2093del (MSH6)	ENSP00000397484.2:p.Glu697del
ENST00000700004.2:c.2388_2390del (MSH6)	ENSP00000514752.2:p.Glu796del
ENST00000699999.1:n.2472_2474del (MSH6)
ENST00000700000.1:c.1606+782_1606+784del (MSH6)	ENSP00000514749.1:n.1606+782_1606+784del
ENST00000700002.1:c.2394_2396del (MSH6)	ENSP00000514750.1:p.Glu798del
ENST00000700003.1:c.628-3049_628-3047del (MSH6)	ENSP00000514751.1:n.628-3049_628-3047del
ENST00000700004.1:c.1545_1547del (MSH6)	ENSP00000514752.1:p.Glu515del
ENST00000234420.11:c.2388_2390del (MSH6) MANE Select	ENSP00000234420.5:p.Glu796del
ENST00000540021.6:c.1998_2000del (MSH6)	ENSP00000446475.1:p.Glu666del
ENST00000652107.1:c.2091_2093del (MSH6)	ENSP00000498629.1:p.Glu697del
ENST00000673637.1:c.2091_2093del (MSH6)	ENSP00000501310.1:p.Glu697del
ENST00000234420.9:c.2388_2390del (MSH6)	ENSP00000234420.4:p.Glu796del
ENST00000405808.5:c.169+7825_169+7827del (FBXO11)	ENSP00000385127.1:n.169+7825_169+7827del
ENST00000434234.5:c.*124+7624_*124+7626del (FBXO11)	ENSP00000402692.1:n.*124+7624_*124+7626del
ENST00000445503.5:c.*1735_*1737del (MSH6)	ENSP00000405294.1:n.*1735_*1737del
ENST00000538136.1:c.1482_1484del (MSH6)	ENSP00000438580.1:p.Glu494del
ENST00000540021.5:c.1998_2000del (MSH6)	ENSP00000446475.1:p.Glu666del
ENST00000614496.4:c.1482_1484del (MSH6)	ENSP00000477844.1:p.Glu494del
ENST00000616033.4:c.2385_2387del (MSH6)	ENSP00000480261.1:p.Glu795del
ENST00000622629.4:c.-709_-707del (MSH6)	ENSP00000482078.1:n.-709_-707del
NM_000179.2:c.2388_2390del , LRG_219t1:c.2388_2390del (MSH6)	NP_000170.1:p.Glu796del
NM_001281492.1:c.1998_2000del (MSH6)	NP_001268421.1:p.Glu666del
NM_001281493.1:c.1482_1484del (MSH6)	NP_001268422.1:p.Glu494del
NM_001281494.1:c.1482_1484del (MSH6)	NP_001268423.1:p.Glu494del
XM_005264271.1:c.2091_2093del (MSH6)	XP_005264328.1:p.Glu697del
XM_011532798.1:c.2205_2207del (MSH6)	XP_011531100.1:p.Glu735del
XM_011532799.1:c.2091_2093del (MSH6)	XP_011531101.1:p.Glu697del
XM_011532800.1:c.2091_2093del (MSH6)	XP_011531102.1:p.Glu697del
XM_024452819.1:c.2388_2390del (MSH6)	XP_024308587.1:p.Glu796del
XM_024452820.1:c.2205_2207del (MSH6)	XP_024308588.1:p.Glu735del
XM_024452821.1:c.2091_2093del (MSH6)	XP_024308589.1:p.Glu697del
XM_024452822.1:c.1482_1484del (MSH6)	XP_024308590.1:p.Glu494del
NM_000179.3:c.2388_2390del (MSH6) MANE Select	NP_000170.1:p.Glu796del
NM_001281492.2:c.1998_2000del (MSH6)	NP_001268421.1:p.Glu666del
NM_001281493.2:c.1482_1484del (MSH6)	NP_001268422.1:p.Glu494del
NM_001281494.2:c.1482_1484del (MSH6)	NP_001268423.1:p.Glu494del