Canonical Allele Identifier: CA10578151

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 234147
• ClinVar RCV Id: RCV000218868 ; RCV000553146 ; RCV000985846 ; RCV004532808
• dbSNP Id: rs876660882
• gnomAD v4: 2-47805668-C-T
• MyVariant Identifiers: chr2:g.48032807C>T (hg19) ; chr2:g.47805668C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805668C>T , CM000664.2:g.47805668C>T	GRCh38
NC_000002.11:g.48032807C>T , CM000664.1:g.48032807C>T	GRCh37
NC_000002.10:g.47886311C>T	NCBI36
NG_007111.1:g.27522C>T , LRG_219:g.27522C>T
NG_008397.1:g.105008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3310C>T (MSH6)	ENSP00000406248.2:p.His1104Tyr
ENST00000420813.6:c.3310C>T (MSH6)	ENSP00000390382.2:p.His1104Tyr
ENST00000455383.6:c.3310C>T (MSH6)	ENSP00000397484.2:p.His1104Tyr
ENST00000700004.2:c.3223C>T (MSH6)	ENSP00000514752.2:p.His1075Tyr
ENST00000699999.1:n.4281C>T (MSH6)
ENST00000700000.1:c.2041C>T (MSH6)	ENSP00000514749.1:p.His681Tyr
ENST00000700002.1:c.3613C>T (MSH6)	ENSP00000514750.1:p.His1205Tyr
ENST00000700003.1:c.1062C>T (MSH6)	ENSP00000514751.1:n.1062C>T
ENST00000700004.1:c.2380C>T (MSH6)	ENSP00000514752.1:p.His794Tyr
ENST00000700005.1:n.2458C>T (MSH6)
ENST00000700006.1:n.4269C>T (MSH6)
ENST00000700007.1:n.2202C>T (MSH6)
ENST00000700008.1:n.1776C>T (MSH6)
ENST00000700009.1:n.1775C>T (MSH6)
ENST00000700010.1:n.1016C>T (MSH6)
ENST00000700011.1:n.2901C>T (MSH6)
ENST00000234420.11:c.3607C>T (MSH6) MANE Select	ENSP00000234420.5:p.His1203Tyr
ENST00000540021.6:c.3217C>T (MSH6)	ENSP00000446475.1:p.His1073Tyr
ENST00000652107.1:c.3310C>T (MSH6)	ENSP00000498629.1:p.His1104Tyr
ENST00000673637.1:c.3310C>T (MSH6)	ENSP00000501310.1:p.His1104Tyr
ENST00000234420.9:c.3607C>T (MSH6)	ENSP00000234420.4:p.His1203Tyr
ENST00000405808.5:c.169+2527G>A (FBXO11)	ENSP00000385127.1:n.169+2527G>A
ENST00000434234.5:c.*124+2326G>A (FBXO11)	ENSP00000402692.1:n.*124+2326G>A
ENST00000445503.5:c.*2954C>T (MSH6)	ENSP00000405294.1:n.*2954C>T
ENST00000538136.1:c.2701C>T (MSH6)	ENSP00000438580.1:p.His901Tyr
ENST00000540021.5:c.3217C>T (MSH6)	ENSP00000446475.1:p.His1073Tyr
ENST00000614496.4:c.2701C>T (MSH6)	ENSP00000477844.1:p.His901Tyr
ENST00000622629.4:c.511C>T (MSH6)	ENSP00000482078.1:p.His171Tyr
NM_000179.2:c.3607C>T , LRG_219t1:c.3607C>T (MSH6)	NP_000170.1:p.His1203Tyr
NM_001281492.1:c.3217C>T (MSH6)	NP_001268421.1:p.His1073Tyr
NM_001281493.1:c.2701C>T (MSH6)	NP_001268422.1:p.His901Tyr
NM_001281494.1:c.2701C>T (MSH6)	NP_001268423.1:p.His901Tyr
XM_005264271.1:c.3310C>T (MSH6)	XP_005264328.1:p.His1104Tyr
XM_011532798.1:c.3424C>T (MSH6)	XP_011531100.1:p.His1142Tyr
XM_011532799.1:c.3310C>T (MSH6)	XP_011531101.1:p.His1104Tyr
XM_011532800.1:c.3310C>T (MSH6)	XP_011531102.1:p.His1104Tyr
XM_024452819.1:c.3607C>T (MSH6)	XP_024308587.1:p.His1203Tyr
XM_024452820.1:c.3424C>T (MSH6)	XP_024308588.1:p.His1142Tyr
XM_024452821.1:c.3310C>T (MSH6)	XP_024308589.1:p.His1104Tyr
XM_024452822.1:c.2701C>T (MSH6)	XP_024308590.1:p.His901Tyr
NM_000179.3:c.3607C>T (MSH6) MANE Select	NP_000170.1:p.His1203Tyr
NM_001281492.2:c.3217C>T (MSH6)	NP_001268421.1:p.His1073Tyr
NM_001281493.2:c.2701C>T (MSH6)	NP_001268422.1:p.His901Tyr
NM_001281494.2:c.2701C>T (MSH6)	NP_001268423.1:p.His901Tyr