Canonical Allele Identifier: CA346761520

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 801224
• ClinVar RCV Id: RCV000985849 ; RCV003594065
• dbSNP Id: rs759092293
• gnomAD v4: 2-47806599-C-T
• MyVariant Identifiers: chr2:g.48033738C>T (hg19) ; chr2:g.47806599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806599C>T , CM000664.2:g.47806599C>T	GRCh38
NC_000002.11:g.48033738C>T , CM000664.1:g.48033738C>T	GRCh37
NC_000002.10:g.47887242C>T	NCBI36
NG_007111.1:g.28453C>T , LRG_219:g.28453C>T
NG_008397.1:g.104077G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3652C>T (MSH6)	ENSP00000406248.2:p.His1218Tyr
ENST00000420813.6:c.3652C>T (MSH6)	ENSP00000390382.2:p.His1218Tyr
ENST00000455383.6:c.3652C>T (MSH6)	ENSP00000397484.2:p.His1218Tyr
ENST00000700004.2:c.3565C>T (MSH6)	ENSP00000514752.2:p.His1189Tyr
ENST00000699999.1:n.4623C>T (MSH6)
ENST00000700000.1:c.2383C>T (MSH6)	ENSP00000514749.1:p.His795Tyr
ENST00000700002.1:c.3955C>T (MSH6)	ENSP00000514750.1:p.His1319Tyr
ENST00000700003.1:c.1404C>T (MSH6)	ENSP00000514751.1:n.1404C>T
ENST00000700004.1:c.2722C>T (MSH6)	ENSP00000514752.1:p.His908Tyr
ENST00000700005.1:n.2800C>T (MSH6)
ENST00000700006.1:n.5107C>T (MSH6)
ENST00000700007.1:n.2544C>T (MSH6)
ENST00000700008.1:n.2211C>T (MSH6)
ENST00000700009.1:n.2613C>T (MSH6)
ENST00000700010.1:n.1358C>T (MSH6)
ENST00000700011.1:n.3243C>T (MSH6)
ENST00000682451.1:n.4149G>A (FBXO11)
ENST00000684712.1:n.4411G>A (FBXO11)
ENST00000234420.11:c.3949C>T (MSH6) MANE Select	ENSP00000234420.5:p.His1317Tyr
ENST00000540021.6:c.3559C>T (MSH6)	ENSP00000446475.1:p.His1187Tyr
ENST00000652107.1:c.3652C>T (MSH6)	ENSP00000498629.1:p.His1218Tyr
ENST00000673637.1:c.3652C>T (MSH6)	ENSP00000501310.1:p.His1218Tyr
ENST00000234420.9:c.3949C>T (MSH6)	ENSP00000234420.4:p.His1317Tyr
ENST00000405808.5:c.169+1596G>A (FBXO11)	ENSP00000385127.1:n.169+1596G>A
ENST00000434234.5:c.*124+1395G>A (FBXO11)	ENSP00000402692.1:n.*124+1395G>A
ENST00000445503.5:c.*3296C>T (MSH6)	ENSP00000405294.1:n.*3296C>T
ENST00000538136.1:c.3043C>T (MSH6)	ENSP00000438580.1:p.His1015Tyr
ENST00000540021.5:c.3559C>T (MSH6)	ENSP00000446475.1:p.His1187Tyr
ENST00000614496.4:c.3043C>T (MSH6)	ENSP00000477844.1:p.His1015Tyr
ENST00000622629.4:c.850C>T (MSH6)	ENSP00000482078.1:p.His284Tyr
NM_000179.2:c.3949C>T , LRG_219t1:c.3949C>T (MSH6)	NP_000170.1:p.His1317Tyr
NM_001281492.1:c.3559C>T (MSH6)	NP_001268421.1:p.His1187Tyr
NM_001281493.1:c.3043C>T (MSH6)	NP_001268422.1:p.His1015Tyr
NM_001281494.1:c.3043C>T (MSH6)	NP_001268423.1:p.His1015Tyr
XM_005264271.1:c.3652C>T (MSH6)	XP_005264328.1:p.His1218Tyr
XM_011532798.1:c.3766C>T (MSH6)	XP_011531100.1:p.His1256Tyr
XM_011532799.1:c.3652C>T (MSH6)	XP_011531101.1:p.His1218Tyr
XM_011532800.1:c.3652C>T (MSH6)	XP_011531102.1:p.His1218Tyr
XM_024452819.1:c.4042C>T (MSH6)	XP_024308587.1:p.His1348Tyr
XM_024452820.1:c.3859C>T (MSH6)	XP_024308588.1:p.His1287Tyr
XM_024452821.1:c.3745C>T (MSH6)	XP_024308589.1:p.His1249Tyr
XM_024452822.1:c.3136C>T (MSH6)	XP_024308590.1:p.His1046Tyr
NM_000179.3:c.3949C>T (MSH6) MANE Select	NP_000170.1:p.His1317Tyr
NM_001281492.2:c.3559C>T (MSH6)	NP_001268421.1:p.His1187Tyr
NM_001281493.2:c.3043C>T (MSH6)	NP_001268422.1:p.His1015Tyr
NM_001281494.2:c.3043C>T (MSH6)	NP_001268423.1:p.His1015Tyr