Canonical Allele Identifier: CA2580067812

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1788883
• ClinVar RCV Id: RCV002446031

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800261_47800279del , CM000664.2:g.47800261_47800279del	GRCh38
NC_000002.11:g.48027400_48027418del , CM000664.1:g.48027400_48027418del	GRCh37
NC_000002.10:g.47880904_47880922del	NCBI36
NG_007111.1:g.22115_22133del , LRG_219:g.22115_22133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1981_1999del (MSH6)	ENSP00000406248.2:p.Glu661IlefsTer9
ENST00000420813.6:c.1981_1999del (MSH6)	ENSP00000390382.2:p.Glu661IlefsTer9
ENST00000455383.6:c.1981_1999del (MSH6)	ENSP00000397484.2:p.Glu661IlefsTer9
ENST00000700004.2:c.2278_2296del (MSH6)	ENSP00000514752.2:p.Glu760IlefsTer9
ENST00000699999.1:n.2362_2380del (MSH6)
ENST00000700000.1:c.1606+672_1606+690del (MSH6)	ENSP00000514749.1:n.1606+672_1606+690del
ENST00000700002.1:c.2284_2302del (MSH6)	ENSP00000514750.1:p.Glu762IlefsTer9
ENST00000700003.1:c.628-3159_628-3141del (MSH6)	ENSP00000514751.1:n.628-3159_628-3141del
ENST00000700004.1:c.1435_1453del (MSH6)	ENSP00000514752.1:p.Glu479IlefsTer9
ENST00000234420.11:c.2278_2296del (MSH6) MANE Select	ENSP00000234420.5:p.Glu760IlefsTer9
ENST00000540021.6:c.1888_1906del (MSH6)	ENSP00000446475.1:p.Glu630IlefsTer9
ENST00000652107.1:c.1981_1999del (MSH6)	ENSP00000498629.1:p.Glu661IlefsTer9
ENST00000673637.1:c.1981_1999del (MSH6)	ENSP00000501310.1:p.Glu661IlefsTer9
ENST00000234420.9:c.2278_2296del (MSH6)	ENSP00000234420.4:p.Glu760IlefsTer9
ENST00000405808.5:c.169+7916_169+7934del (FBXO11)	ENSP00000385127.1:n.169+7916_169+7934del
ENST00000434234.5:c.*124+7715_*124+7733del (FBXO11)	ENSP00000402692.1:n.*124+7715_*124+7733del
ENST00000445503.5:c.*1625_*1643del (MSH6)	ENSP00000405294.1:n.*1625_*1643del
ENST00000538136.1:c.1372_1390del (MSH6)	ENSP00000438580.1:p.Glu458IlefsTer9
ENST00000540021.5:c.1888_1906del (MSH6)	ENSP00000446475.1:p.Glu630IlefsTer9
ENST00000614496.4:c.1372_1390del (MSH6)	ENSP00000477844.1:p.Glu458IlefsTer9
ENST00000616033.4:c.2275_2293del (MSH6)	ENSP00000480261.1:p.Glu759IlefsTer9
ENST00000622629.4:c.-819_-801del (MSH6)	ENSP00000482078.1:n.-819_-801del
NM_000179.2:c.2278_2296del , LRG_219t1:c.2278_2296del (MSH6)	NP_000170.1:p.Glu760IlefsTer9
NM_001281492.1:c.1888_1906del (MSH6)	NP_001268421.1:p.Glu630IlefsTer9
NM_001281493.1:c.1372_1390del (MSH6)	NP_001268422.1:p.Glu458IlefsTer9
NM_001281494.1:c.1372_1390del (MSH6)	NP_001268423.1:p.Glu458IlefsTer9
XM_005264271.1:c.1981_1999del (MSH6)	XP_005264328.1:p.Glu661IlefsTer9
XM_011532798.1:c.2095_2113del (MSH6)	XP_011531100.1:p.Glu699IlefsTer9
XM_011532799.1:c.1981_1999del (MSH6)	XP_011531101.1:p.Glu661IlefsTer9
XM_011532800.1:c.1981_1999del (MSH6)	XP_011531102.1:p.Glu661IlefsTer9
XM_024452819.1:c.2278_2296del (MSH6)	XP_024308587.1:p.Glu760IlefsTer9
XM_024452820.1:c.2095_2113del (MSH6)	XP_024308588.1:p.Glu699IlefsTer9
XM_024452821.1:c.1981_1999del (MSH6)	XP_024308589.1:p.Glu661IlefsTer9
XM_024452822.1:c.1372_1390del (MSH6)	XP_024308590.1:p.Glu458IlefsTer9
NM_000179.3:c.2278_2296del (MSH6) MANE Select	NP_000170.1:p.Glu760IlefsTer9
NM_001281492.2:c.1888_1906del (MSH6)	NP_001268421.1:p.Glu630IlefsTer9
NM_001281493.2:c.1372_1390del (MSH6)	NP_001268422.1:p.Glu458IlefsTer9
NM_001281494.2:c.1372_1390del (MSH6)	NP_001268423.1:p.Glu458IlefsTer9