Canonical Allele Identifier: CA346761478

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48033718A>G (hg19) ; chr2:g.47806579A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806579A>G , CM000664.2:g.47806579A>G	GRCh38
NC_000002.11:g.48033718A>G , CM000664.1:g.48033718A>G	GRCh37
NC_000002.10:g.47887222A>G	NCBI36
NG_007111.1:g.28433A>G , LRG_219:g.28433A>G
NG_008397.1:g.104097T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3632A>G (MSH6)	ENSP00000406248.2:p.Glu1211Gly
ENST00000420813.6:c.3632A>G (MSH6)	ENSP00000390382.2:p.Glu1211Gly
ENST00000455383.6:c.3632A>G (MSH6)	ENSP00000397484.2:p.Glu1211Gly
ENST00000700004.2:c.3545A>G (MSH6)	ENSP00000514752.2:p.Glu1182Gly
ENST00000699999.1:n.4603A>G (MSH6)
ENST00000700000.1:c.2363A>G (MSH6)	ENSP00000514749.1:p.Glu788Gly
ENST00000700002.1:c.3935A>G (MSH6)	ENSP00000514750.1:p.Glu1312Gly
ENST00000700003.1:c.1384A>G (MSH6)	ENSP00000514751.1:n.1384A>G
ENST00000700004.1:c.2702A>G (MSH6)	ENSP00000514752.1:p.Glu901Gly
ENST00000700005.1:n.2780A>G (MSH6)
ENST00000700006.1:n.5087A>G (MSH6)
ENST00000700007.1:n.2524A>G (MSH6)
ENST00000700008.1:n.2191A>G (MSH6)
ENST00000700009.1:n.2593A>G (MSH6)
ENST00000700010.1:n.1338A>G (MSH6)
ENST00000700011.1:n.3223A>G (MSH6)
ENST00000682451.1:n.4169T>C (FBXO11)
ENST00000684712.1:n.4431T>C (FBXO11)
ENST00000234420.11:c.3929A>G (MSH6) MANE Select	ENSP00000234420.5:p.Glu1310Gly
ENST00000540021.6:c.3539A>G (MSH6)	ENSP00000446475.1:p.Glu1180Gly
ENST00000652107.1:c.3632A>G (MSH6)	ENSP00000498629.1:p.Glu1211Gly
ENST00000673637.1:c.3632A>G (MSH6)	ENSP00000501310.1:p.Glu1211Gly
ENST00000234420.9:c.3929A>G (MSH6)	ENSP00000234420.4:p.Glu1310Gly
ENST00000405808.5:c.169+1616T>C (FBXO11)	ENSP00000385127.1:n.169+1616T>C
ENST00000434234.5:c.*124+1415T>C (FBXO11)	ENSP00000402692.1:n.*124+1415T>C
ENST00000445503.5:c.*3276A>G (MSH6)	ENSP00000405294.1:n.*3276A>G
ENST00000538136.1:c.3023A>G (MSH6)	ENSP00000438580.1:p.Glu1008Gly
ENST00000540021.5:c.3539A>G (MSH6)	ENSP00000446475.1:p.Glu1180Gly
ENST00000614496.4:c.3023A>G (MSH6)	ENSP00000477844.1:p.Glu1008Gly
ENST00000622629.4:c.830A>G (MSH6)	ENSP00000482078.1:p.Glu277Gly
NM_000179.2:c.3929A>G , LRG_219t1:c.3929A>G (MSH6)	NP_000170.1:p.Glu1310Gly
NM_001281492.1:c.3539A>G (MSH6)	NP_001268421.1:p.Glu1180Gly
NM_001281493.1:c.3023A>G (MSH6)	NP_001268422.1:p.Glu1008Gly
NM_001281494.1:c.3023A>G (MSH6)	NP_001268423.1:p.Glu1008Gly
XM_005264271.1:c.3632A>G (MSH6)	XP_005264328.1:p.Glu1211Gly
XM_011532798.1:c.3746A>G (MSH6)	XP_011531100.1:p.Glu1249Gly
XM_011532799.1:c.3632A>G (MSH6)	XP_011531101.1:p.Glu1211Gly
XM_011532800.1:c.3632A>G (MSH6)	XP_011531102.1:p.Glu1211Gly
XM_024452819.1:c.4022A>G (MSH6)	XP_024308587.1:p.Glu1341Gly
XM_024452820.1:c.3839A>G (MSH6)	XP_024308588.1:p.Glu1280Gly
XM_024452821.1:c.3725A>G (MSH6)	XP_024308589.1:p.Glu1242Gly
XM_024452822.1:c.3116A>G (MSH6)	XP_024308590.1:p.Glu1039Gly
NM_000179.3:c.3929A>G (MSH6) MANE Select	NP_000170.1:p.Glu1310Gly
NM_001281492.2:c.3539A>G (MSH6)	NP_001268421.1:p.Glu1180Gly
NM_001281493.2:c.3023A>G (MSH6)	NP_001268422.1:p.Glu1008Gly
NM_001281494.2:c.3023A>G (MSH6)	NP_001268423.1:p.Glu1008Gly