Canonical Allele Identifier: CA346760507

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48032778A>G (hg19) ; chr2:g.47805639A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805639A>G , CM000664.2:g.47805639A>G	GRCh38
NC_000002.11:g.48032778A>G , CM000664.1:g.48032778A>G	GRCh37
NC_000002.10:g.47886282A>G	NCBI36
NG_007111.1:g.27493A>G , LRG_219:g.27493A>G
NG_008397.1:g.105037T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3281A>G (MSH6)	ENSP00000406248.2:p.Glu1094Gly
ENST00000420813.6:c.3281A>G (MSH6)	ENSP00000390382.2:p.Glu1094Gly
ENST00000455383.6:c.3281A>G (MSH6)	ENSP00000397484.2:p.Glu1094Gly
ENST00000700004.2:c.3194A>G (MSH6)	ENSP00000514752.2:p.Glu1065Gly
ENST00000699999.1:n.4252A>G (MSH6)
ENST00000700000.1:c.2012A>G (MSH6)	ENSP00000514749.1:p.Glu671Gly
ENST00000700002.1:c.3584A>G (MSH6)	ENSP00000514750.1:p.Glu1195Gly
ENST00000700003.1:c.1033A>G (MSH6)	ENSP00000514751.1:n.1033A>G
ENST00000700004.1:c.2351A>G (MSH6)	ENSP00000514752.1:p.Glu784Gly
ENST00000700005.1:n.2429A>G (MSH6)
ENST00000700006.1:n.4240A>G (MSH6)
ENST00000700007.1:n.2173A>G (MSH6)
ENST00000700008.1:n.1747A>G (MSH6)
ENST00000700009.1:n.1746A>G (MSH6)
ENST00000700010.1:n.987A>G (MSH6)
ENST00000700011.1:n.2872A>G (MSH6)
ENST00000234420.11:c.3578A>G (MSH6) MANE Select	ENSP00000234420.5:p.Glu1193Gly
ENST00000540021.6:c.3188A>G (MSH6)	ENSP00000446475.1:p.Glu1063Gly
ENST00000652107.1:c.3281A>G (MSH6)	ENSP00000498629.1:p.Glu1094Gly
ENST00000673637.1:c.3281A>G (MSH6)	ENSP00000501310.1:p.Glu1094Gly
ENST00000234420.9:c.3578A>G (MSH6)	ENSP00000234420.4:p.Glu1193Gly
ENST00000405808.5:c.169+2556T>C (FBXO11)	ENSP00000385127.1:n.169+2556T>C
ENST00000434234.5:c.*124+2355T>C (FBXO11)	ENSP00000402692.1:n.*124+2355T>C
ENST00000445503.5:c.*2925A>G (MSH6)	ENSP00000405294.1:n.*2925A>G
ENST00000538136.1:c.2672A>G (MSH6)	ENSP00000438580.1:p.Glu891Gly
ENST00000540021.5:c.3188A>G (MSH6)	ENSP00000446475.1:p.Glu1063Gly
ENST00000614496.4:c.2672A>G (MSH6)	ENSP00000477844.1:p.Glu891Gly
ENST00000622629.4:c.482A>G (MSH6)	ENSP00000482078.1:p.Glu161Gly
NM_000179.2:c.3578A>G , LRG_219t1:c.3578A>G (MSH6)	NP_000170.1:p.Glu1193Gly
NM_001281492.1:c.3188A>G (MSH6)	NP_001268421.1:p.Glu1063Gly
NM_001281493.1:c.2672A>G (MSH6)	NP_001268422.1:p.Glu891Gly
NM_001281494.1:c.2672A>G (MSH6)	NP_001268423.1:p.Glu891Gly
XM_005264271.1:c.3281A>G (MSH6)	XP_005264328.1:p.Glu1094Gly
XM_011532798.1:c.3395A>G (MSH6)	XP_011531100.1:p.Glu1132Gly
XM_011532799.1:c.3281A>G (MSH6)	XP_011531101.1:p.Glu1094Gly
XM_011532800.1:c.3281A>G (MSH6)	XP_011531102.1:p.Glu1094Gly
XM_024452819.1:c.3578A>G (MSH6)	XP_024308587.1:p.Glu1193Gly
XM_024452820.1:c.3395A>G (MSH6)	XP_024308588.1:p.Glu1132Gly
XM_024452821.1:c.3281A>G (MSH6)	XP_024308589.1:p.Glu1094Gly
XM_024452822.1:c.2672A>G (MSH6)	XP_024308590.1:p.Glu891Gly
NM_000179.3:c.3578A>G (MSH6) MANE Select	NP_000170.1:p.Glu1193Gly
NM_001281492.2:c.3188A>G (MSH6)	NP_001268421.1:p.Glu1063Gly
NM_001281493.2:c.2672A>G (MSH6)	NP_001268422.1:p.Glu891Gly
NM_001281494.2:c.2672A>G (MSH6)	NP_001268423.1:p.Glu891Gly