Canonical Allele Identifier: CA346761188

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1025468
• ClinVar RCV Id: RCV001325782 ; RCV002366203
• dbSNP Id: rs972387746
• gnomAD v4: 2-47806353-C-G
• MyVariant Identifiers: chr2:g.48033492C>G (hg19) ; chr2:g.47806353C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806353C>G , CM000664.2:g.47806353C>G	GRCh38
NC_000002.11:g.48033492C>G , CM000664.1:g.48033492C>G	GRCh37
NC_000002.10:g.47886996C>G	NCBI36
NG_007111.1:g.28207C>G , LRG_219:g.28207C>G
NG_008397.1:g.104323G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3499C>G (MSH6)	ENSP00000406248.2:p.His1167Asp
ENST00000420813.6:c.3499C>G (MSH6)	ENSP00000390382.2:p.His1167Asp
ENST00000455383.6:c.3499C>G (MSH6)	ENSP00000397484.2:p.His1167Asp
ENST00000700004.2:c.3412C>G (MSH6)	ENSP00000514752.2:p.His1138Asp
ENST00000699999.1:n.4470C>G (MSH6)
ENST00000700000.1:c.2230C>G (MSH6)	ENSP00000514749.1:p.His744Asp
ENST00000700002.1:c.3802C>G (MSH6)	ENSP00000514750.1:p.His1268Asp
ENST00000700003.1:c.1251C>G (MSH6)	ENSP00000514751.1:n.1251C>G
ENST00000700004.1:c.2569C>G (MSH6)	ENSP00000514752.1:p.His857Asp
ENST00000700005.1:n.2647C>G (MSH6)
ENST00000700006.1:n.4954C>G (MSH6)
ENST00000700007.1:n.2391C>G (MSH6)
ENST00000700008.1:n.1965C>G (MSH6)
ENST00000700009.1:n.2460C>G (MSH6)
ENST00000700010.1:n.1205C>G (MSH6)
ENST00000700011.1:n.3090C>G (MSH6)
ENST00000682451.1:n.4395G>C (FBXO11)
ENST00000684712.1:n.4657G>C (FBXO11)
ENST00000234420.11:c.3796C>G (MSH6) MANE Select	ENSP00000234420.5:p.His1266Asp
ENST00000540021.6:c.3406C>G (MSH6)	ENSP00000446475.1:p.His1136Asp
ENST00000652107.1:c.3499C>G (MSH6)	ENSP00000498629.1:p.His1167Asp
ENST00000673637.1:c.3499C>G (MSH6)	ENSP00000501310.1:p.His1167Asp
ENST00000234420.9:c.3796C>G (MSH6)	ENSP00000234420.4:p.His1266Asp
ENST00000405808.5:c.169+1842G>C (FBXO11)	ENSP00000385127.1:n.169+1842G>C
ENST00000434234.5:c.*124+1641G>C (FBXO11)	ENSP00000402692.1:n.*124+1641G>C
ENST00000445503.5:c.*3143C>G (MSH6)	ENSP00000405294.1:n.*3143C>G
ENST00000538136.1:c.2890C>G (MSH6)	ENSP00000438580.1:p.His964Asp
ENST00000540021.5:c.3406C>G (MSH6)	ENSP00000446475.1:p.His1136Asp
ENST00000614496.4:c.2890C>G (MSH6)	ENSP00000477844.1:p.His964Asp
ENST00000622629.4:c.697C>G (MSH6)	ENSP00000482078.1:p.His233Asp
NM_000179.2:c.3796C>G , LRG_219t1:c.3796C>G (MSH6)	NP_000170.1:p.His1266Asp
NM_001281492.1:c.3406C>G (MSH6)	NP_001268421.1:p.His1136Asp
NM_001281493.1:c.2890C>G (MSH6)	NP_001268422.1:p.His964Asp
NM_001281494.1:c.2890C>G (MSH6)	NP_001268423.1:p.His964Asp
XM_005264271.1:c.3499C>G (MSH6)	XP_005264328.1:p.His1167Asp
XM_011532798.1:c.3613C>G (MSH6)	XP_011531100.1:p.His1205Asp
XM_011532799.1:c.3499C>G (MSH6)	XP_011531101.1:p.His1167Asp
XM_011532800.1:c.3499C>G (MSH6)	XP_011531102.1:p.His1167Asp
XM_024452819.1:c.3796C>G (MSH6)	XP_024308587.1:p.His1266Asp
XM_024452820.1:c.3613C>G (MSH6)	XP_024308588.1:p.His1205Asp
XM_024452821.1:c.3499C>G (MSH6)	XP_024308589.1:p.His1167Asp
XM_024452822.1:c.2890C>G (MSH6)	XP_024308590.1:p.His964Asp
NM_000179.3:c.3796C>G (MSH6) MANE Select	NP_000170.1:p.His1266Asp
NM_001281492.2:c.3406C>G (MSH6)	NP_001268421.1:p.His1136Asp
NM_001281493.2:c.2890C>G (MSH6)	NP_001268422.1:p.His964Asp
NM_001281494.2:c.2890C>G (MSH6)	NP_001268423.1:p.His964Asp