Canonical Allele Identifier: CA346760465

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 581918
• ClinVar RCV Id: RCV000705873 ; RCV003165915
• dbSNP Id: rs778651272
• gnomAD v4: 2-47805629-T-G
• MyVariant Identifiers: chr2:g.48032768T>G (hg19) ; chr2:g.47805629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805629T>G , CM000664.2:g.47805629T>G	GRCh38
NC_000002.11:g.48032768T>G , CM000664.1:g.48032768T>G	GRCh37
NC_000002.10:g.47886272T>G	NCBI36
NG_007111.1:g.27483T>G , LRG_219:g.27483T>G
NG_008397.1:g.105047A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3271T>G (MSH6)	ENSP00000406248.2:p.Phe1091Val
ENST00000420813.6:c.3271T>G (MSH6)	ENSP00000390382.2:p.Phe1091Val
ENST00000455383.6:c.3271T>G (MSH6)	ENSP00000397484.2:p.Phe1091Val
ENST00000700004.2:c.3184T>G (MSH6)	ENSP00000514752.2:p.Phe1062Val
ENST00000699999.1:n.4242T>G (MSH6)
ENST00000700000.1:c.2002T>G (MSH6)	ENSP00000514749.1:p.Phe668Val
ENST00000700002.1:c.3574T>G (MSH6)	ENSP00000514750.1:p.Phe1192Val
ENST00000700003.1:c.1023T>G (MSH6)	ENSP00000514751.1:n.1023T>G
ENST00000700004.1:c.2341T>G (MSH6)	ENSP00000514752.1:p.Phe781Val
ENST00000700005.1:n.2419T>G (MSH6)
ENST00000700006.1:n.4230T>G (MSH6)
ENST00000700007.1:n.2163T>G (MSH6)
ENST00000700008.1:n.1737T>G (MSH6)
ENST00000700009.1:n.1736T>G (MSH6)
ENST00000700010.1:n.977T>G (MSH6)
ENST00000700011.1:n.2862T>G (MSH6)
ENST00000234420.11:c.3568T>G (MSH6) MANE Select	ENSP00000234420.5:p.Phe1190Val
ENST00000540021.6:c.3178T>G (MSH6)	ENSP00000446475.1:p.Phe1060Val
ENST00000652107.1:c.3271T>G (MSH6)	ENSP00000498629.1:p.Phe1091Val
ENST00000673637.1:c.3271T>G (MSH6)	ENSP00000501310.1:p.Phe1091Val
ENST00000234420.9:c.3568T>G (MSH6)	ENSP00000234420.4:p.Phe1190Val
ENST00000405808.5:c.169+2566A>C (FBXO11)	ENSP00000385127.1:n.169+2566A>C
ENST00000434234.5:c.*124+2365A>C (FBXO11)	ENSP00000402692.1:n.*124+2365A>C
ENST00000445503.5:c.*2915T>G (MSH6)	ENSP00000405294.1:n.*2915T>G
ENST00000538136.1:c.2662T>G (MSH6)	ENSP00000438580.1:p.Phe888Val
ENST00000540021.5:c.3178T>G (MSH6)	ENSP00000446475.1:p.Phe1060Val
ENST00000614496.4:c.2662T>G (MSH6)	ENSP00000477844.1:p.Phe888Val
ENST00000622629.4:c.472T>G (MSH6)	ENSP00000482078.1:p.Phe158Val
NM_000179.2:c.3568T>G , LRG_219t1:c.3568T>G (MSH6)	NP_000170.1:p.Phe1190Val
NM_001281492.1:c.3178T>G (MSH6)	NP_001268421.1:p.Phe1060Val
NM_001281493.1:c.2662T>G (MSH6)	NP_001268422.1:p.Phe888Val
NM_001281494.1:c.2662T>G (MSH6)	NP_001268423.1:p.Phe888Val
XM_005264271.1:c.3271T>G (MSH6)	XP_005264328.1:p.Phe1091Val
XM_011532798.1:c.3385T>G (MSH6)	XP_011531100.1:p.Phe1129Val
XM_011532799.1:c.3271T>G (MSH6)	XP_011531101.1:p.Phe1091Val
XM_011532800.1:c.3271T>G (MSH6)	XP_011531102.1:p.Phe1091Val
XM_024452819.1:c.3568T>G (MSH6)	XP_024308587.1:p.Phe1190Val
XM_024452820.1:c.3385T>G (MSH6)	XP_024308588.1:p.Phe1129Val
XM_024452821.1:c.3271T>G (MSH6)	XP_024308589.1:p.Phe1091Val
XM_024452822.1:c.2662T>G (MSH6)	XP_024308590.1:p.Phe888Val
NM_000179.3:c.3568T>G (MSH6) MANE Select	NP_000170.1:p.Phe1190Val
NM_001281492.2:c.3178T>G (MSH6)	NP_001268421.1:p.Phe1060Val
NM_001281493.2:c.2662T>G (MSH6)	NP_001268422.1:p.Phe888Val
NM_001281494.2:c.2662T>G (MSH6)	NP_001268423.1:p.Phe888Val