Canonical Allele Identifier: CA2496049640

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 997867
• ClinVar RCV Id: RCV001293484
• dbSNP Id: rs1669481204

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800549_47800555del , CM000664.2:g.47800549_47800555del	GRCh38
NC_000002.11:g.48027688_48027694del , CM000664.1:g.48027688_48027694del	GRCh37
NC_000002.10:g.47881192_47881198del	NCBI36
NG_007111.1:g.22403_22409del , LRG_219:g.22403_22409del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2269_2275del (MSH6)	ENSP00000406248.2:p.Ile757PhefsTer10
ENST00000420813.6:c.2269_2275del (MSH6)	ENSP00000390382.2:p.Ile757PhefsTer10
ENST00000455383.6:c.2269_2275del (MSH6)	ENSP00000397484.2:p.Ile757PhefsTer10
ENST00000700004.2:c.2566_2572del (MSH6)	ENSP00000514752.2:p.Ile856PhefsTer10
ENST00000699999.1:n.2650_2656del (MSH6)
ENST00000700000.1:c.1606+960_1606+966del (MSH6)	ENSP00000514749.1:n.1606+960_1606+966del
ENST00000700002.1:c.2572_2578del (MSH6)	ENSP00000514750.1:p.Ile858PhefsTer10
ENST00000700003.1:c.628-2871_628-2865del (MSH6)	ENSP00000514751.1:n.628-2871_628-2865del
ENST00000700004.1:c.1723_1729del (MSH6)	ENSP00000514752.1:p.Ile575PhefsTer10
ENST00000234420.11:c.2566_2572del (MSH6) MANE Select	ENSP00000234420.5:p.Ile856PhefsTer10
ENST00000540021.6:c.2176_2182del (MSH6)	ENSP00000446475.1:p.Ile726PhefsTer10
ENST00000652107.1:c.2269_2275del (MSH6)	ENSP00000498629.1:p.Ile757PhefsTer10
ENST00000673637.1:c.2269_2275del (MSH6)	ENSP00000501310.1:p.Ile757PhefsTer10
ENST00000234420.9:c.2566_2572del (MSH6)	ENSP00000234420.4:p.Ile856PhefsTer10
ENST00000405808.5:c.169+7644_169+7650del (FBXO11)	ENSP00000385127.1:n.169+7644_169+7650del
ENST00000434234.5:c.*124+7443_*124+7449del (FBXO11)	ENSP00000402692.1:n.*124+7443_*124+7449de...
ENST00000445503.5:c.*1913_*1919del (MSH6)	ENSP00000405294.1:n.*1913_*1919del
ENST00000538136.1:c.1660_1666del (MSH6)	ENSP00000438580.1:p.Ile554PhefsTer10
ENST00000540021.5:c.2176_2182del (MSH6)	ENSP00000446475.1:p.Ile726PhefsTer10
ENST00000614496.4:c.1660_1666del (MSH6)	ENSP00000477844.1:p.Ile554PhefsTer10
ENST00000616033.4:c.2563_2569del (MSH6)	ENSP00000480261.1:p.Ile855PhefsTer10
ENST00000622629.4:c.-531_-525del (MSH6)	ENSP00000482078.1:n.-531_-525del
NM_000179.2:c.2566_2572del , LRG_219t1:c.2566_2572del (MSH6)	NP_000170.1:p.Ile856PhefsTer10
NM_001281492.1:c.2176_2182del (MSH6)	NP_001268421.1:p.Ile726PhefsTer10
NM_001281493.1:c.1660_1666del (MSH6)	NP_001268422.1:p.Ile554PhefsTer10
NM_001281494.1:c.1660_1666del (MSH6)	NP_001268423.1:p.Ile554PhefsTer10
XM_005264271.1:c.2269_2275del (MSH6)	XP_005264328.1:p.Ile757PhefsTer10
XM_011532798.1:c.2383_2389del (MSH6)	XP_011531100.1:p.Ile795PhefsTer10
XM_011532799.1:c.2269_2275del (MSH6)	XP_011531101.1:p.Ile757PhefsTer10
XM_011532800.1:c.2269_2275del (MSH6)	XP_011531102.1:p.Ile757PhefsTer10
XM_024452819.1:c.2566_2572del (MSH6)	XP_024308587.1:p.Ile856PhefsTer10
XM_024452820.1:c.2383_2389del (MSH6)	XP_024308588.1:p.Ile795PhefsTer10
XM_024452821.1:c.2269_2275del (MSH6)	XP_024308589.1:p.Ile757PhefsTer10
XM_024452822.1:c.1660_1666del (MSH6)	XP_024308590.1:p.Ile554PhefsTer10
NM_000179.3:c.2566_2572del (MSH6) MANE Select	NP_000170.1:p.Ile856PhefsTer10
NM_001281492.2:c.2176_2182del (MSH6)	NP_001268421.1:p.Ile726PhefsTer10
NM_001281493.2:c.1660_1666del (MSH6)	NP_001268422.1:p.Ile554PhefsTer10
NM_001281494.2:c.1660_1666del (MSH6)	NP_001268423.1:p.Ile554PhefsTer10