Canonical Allele Identifier: CA346761133

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48033469A>G (hg19) ; chr2:g.47806330A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806330A>G , CM000664.2:g.47806330A>G	GRCh38
NC_000002.11:g.48033469A>G , CM000664.1:g.48033469A>G	GRCh37
NC_000002.10:g.47886973A>G	NCBI36
NG_007111.1:g.28184A>G , LRG_219:g.28184A>G
NG_008397.1:g.104346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3476A>G (MSH6)	ENSP00000406248.2:p.Gln1159Arg
ENST00000420813.6:c.3476A>G (MSH6)	ENSP00000390382.2:p.Gln1159Arg
ENST00000455383.6:c.3476A>G (MSH6)	ENSP00000397484.2:p.Gln1159Arg
ENST00000700004.2:c.3389A>G (MSH6)	ENSP00000514752.2:p.Gln1130Arg
ENST00000699999.1:n.4447A>G (MSH6)
ENST00000700000.1:c.2207A>G (MSH6)	ENSP00000514749.1:p.Gln736Arg
ENST00000700002.1:c.3779A>G (MSH6)	ENSP00000514750.1:p.Gln1260Arg
ENST00000700003.1:c.1228A>G (MSH6)	ENSP00000514751.1:n.1228A>G
ENST00000700004.1:c.2546A>G (MSH6)	ENSP00000514752.1:p.Gln849Arg
ENST00000700005.1:n.2624A>G (MSH6)
ENST00000700006.1:n.4931A>G (MSH6)
ENST00000700007.1:n.2368A>G (MSH6)
ENST00000700008.1:n.1942A>G (MSH6)
ENST00000700009.1:n.2437A>G (MSH6)
ENST00000700010.1:n.1182A>G (MSH6)
ENST00000700011.1:n.3067A>G (MSH6)
ENST00000682451.1:n.4418T>C (FBXO11)
ENST00000684712.1:n.4680T>C (FBXO11)
ENST00000234420.11:c.3773A>G (MSH6) MANE Select	ENSP00000234420.5:p.Gln1258Arg
ENST00000540021.6:c.3383A>G (MSH6)	ENSP00000446475.1:p.Gln1128Arg
ENST00000652107.1:c.3476A>G (MSH6)	ENSP00000498629.1:p.Gln1159Arg
ENST00000673637.1:c.3476A>G (MSH6)	ENSP00000501310.1:p.Gln1159Arg
ENST00000234420.9:c.3773A>G (MSH6)	ENSP00000234420.4:p.Gln1258Arg
ENST00000405808.5:c.169+1865T>C (FBXO11)	ENSP00000385127.1:n.169+1865T>C
ENST00000434234.5:c.*124+1664T>C (FBXO11)	ENSP00000402692.1:n.*124+1664T>C
ENST00000445503.5:c.*3120A>G (MSH6)	ENSP00000405294.1:n.*3120A>G
ENST00000538136.1:c.2867A>G (MSH6)	ENSP00000438580.1:p.Gln956Arg
ENST00000540021.5:c.3383A>G (MSH6)	ENSP00000446475.1:p.Gln1128Arg
ENST00000614496.4:c.2867A>G (MSH6)	ENSP00000477844.1:p.Gln956Arg
ENST00000622629.4:c.675A>G (MSH6)	ENSP00000482078.1:p.Ser225=
NM_000179.2:c.3773A>G , LRG_219t1:c.3773A>G (MSH6)	NP_000170.1:p.Gln1258Arg
NM_001281492.1:c.3383A>G (MSH6)	NP_001268421.1:p.Gln1128Arg
NM_001281493.1:c.2867A>G (MSH6)	NP_001268422.1:p.Gln956Arg
NM_001281494.1:c.2867A>G (MSH6)	NP_001268423.1:p.Gln956Arg
XM_005264271.1:c.3476A>G (MSH6)	XP_005264328.1:p.Gln1159Arg
XM_011532798.1:c.3590A>G (MSH6)	XP_011531100.1:p.Gln1197Arg
XM_011532799.1:c.3476A>G (MSH6)	XP_011531101.1:p.Gln1159Arg
XM_011532800.1:c.3476A>G (MSH6)	XP_011531102.1:p.Gln1159Arg
XM_024452819.1:c.3773A>G (MSH6)	XP_024308587.1:p.Gln1258Arg
XM_024452820.1:c.3590A>G (MSH6)	XP_024308588.1:p.Gln1197Arg
XM_024452821.1:c.3476A>G (MSH6)	XP_024308589.1:p.Gln1159Arg
XM_024452822.1:c.2867A>G (MSH6)	XP_024308590.1:p.Gln956Arg
NM_000179.3:c.3773A>G (MSH6) MANE Select	NP_000170.1:p.Gln1258Arg
NM_001281492.2:c.3383A>G (MSH6)	NP_001268421.1:p.Gln1128Arg
NM_001281493.2:c.2867A>G (MSH6)	NP_001268422.1:p.Gln956Arg
NM_001281494.2:c.2867A>G (MSH6)	NP_001268423.1:p.Gln956Arg