Canonical Allele Identifier: CA2580067579

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1771267
• ClinVar RCV Id: RCV002381145

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799363_47799365del , CM000664.2:g.47799363_47799365del	GRCh38
NC_000002.11:g.48026502_48026504del , CM000664.1:g.48026502_48026504del	GRCh37
NC_000002.10:g.47880006_47880008del	NCBI36
NG_007111.1:g.21217_21219del , LRG_219:g.21217_21219del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1083_1085del (MSH6)	ENSP00000406248.2:p.Phe362del
ENST00000420813.6:c.1083_1085del (MSH6)	ENSP00000390382.2:p.Phe362del
ENST00000455383.6:c.1083_1085del (MSH6)	ENSP00000397484.2:p.Phe362del
ENST00000700004.2:c.1380_1382del (MSH6)	ENSP00000514752.2:p.Phe461del
ENST00000699999.1:n.1464_1466del (MSH6)
ENST00000700000.1:c.1380_1382del (MSH6)	ENSP00000514749.1:p.Phe461del
ENST00000700002.1:c.1386_1388del (MSH6)	ENSP00000514750.1:p.Phe463del
ENST00000700003.1:c.627+3300_627+3302del (MSH6)	ENSP00000514751.1:n.627+3300_627+3302del
ENST00000700004.1:c.537_539del (MSH6)	ENSP00000514752.1:p.Phe180del
ENST00000234420.11:c.1380_1382del (MSH6) MANE Select	ENSP00000234420.5:p.Phe461del
ENST00000540021.6:c.990_992del (MSH6)	ENSP00000446475.1:p.Phe331del
ENST00000652107.1:c.1083_1085del (MSH6)	ENSP00000498629.1:p.Phe362del
ENST00000673637.1:c.1083_1085del (MSH6)	ENSP00000501310.1:p.Phe362del
ENST00000234420.9:c.1380_1382del (MSH6)	ENSP00000234420.4:p.Phe461del
ENST00000405808.5:c.169+8830_169+8832del (FBXO11)	ENSP00000385127.1:n.169+8830_169+8832del
ENST00000434234.5:c.*124+8629_*124+8631del (FBXO11)	ENSP00000402692.1:n.*124+8629_*124+8631de...
ENST00000445503.5:c.*727_*729del (MSH6)	ENSP00000405294.1:n.*727_*729del
ENST00000538136.1:c.474_476del (MSH6)	ENSP00000438580.1:p.Phe159del
ENST00000540021.5:c.990_992del (MSH6)	ENSP00000446475.1:p.Phe331del
ENST00000614496.4:c.474_476del (MSH6)	ENSP00000477844.1:p.Phe159del
ENST00000616033.4:c.1377_1379del (MSH6)	ENSP00000480261.1:p.Phe460del
ENST00000622629.4:c.-1717_-1715del (MSH6)	ENSP00000482078.1:n.-1717_-1715del
NM_000179.2:c.1380_1382del , LRG_219t1:c.1380_1382del (MSH6)	NP_000170.1:p.Phe461del
NM_001281492.1:c.990_992del (MSH6)	NP_001268421.1:p.Phe331del
NM_001281493.1:c.474_476del (MSH6)	NP_001268422.1:p.Phe159del
NM_001281494.1:c.474_476del (MSH6)	NP_001268423.1:p.Phe159del
XM_005264271.1:c.1083_1085del (MSH6)	XP_005264328.1:p.Phe362del
XM_011532798.1:c.1197_1199del (MSH6)	XP_011531100.1:p.Phe400del
XM_011532799.1:c.1083_1085del (MSH6)	XP_011531101.1:p.Phe362del
XM_011532800.1:c.1083_1085del (MSH6)	XP_011531102.1:p.Phe362del
XM_024452819.1:c.1380_1382del (MSH6)	XP_024308587.1:p.Phe461del
XM_024452820.1:c.1197_1199del (MSH6)	XP_024308588.1:p.Phe400del
XM_024452821.1:c.1083_1085del (MSH6)	XP_024308589.1:p.Phe362del
XM_024452822.1:c.474_476del (MSH6)	XP_024308590.1:p.Phe159del
NM_000179.3:c.1380_1382del (MSH6) MANE Select	NP_000170.1:p.Phe461del
NM_001281492.2:c.990_992del (MSH6)	NP_001268421.1:p.Phe331del
NM_001281493.2:c.474_476del (MSH6)	NP_001268422.1:p.Phe159del
NM_001281494.2:c.474_476del (MSH6)	NP_001268423.1:p.Phe159del