Canonical Allele Identifier: CA014672

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 185639
• ClinVar RCV Id: RCV000165091
• dbSNP Id: rs786202333
• MyVariant Identifiers: chr2:g.48033701G>T (hg19) ; chr2:g.47806562G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806562G>T , CM000664.2:g.47806562G>T	GRCh38
NC_000002.11:g.48033701G>T , CM000664.1:g.48033701G>T	GRCh37
NC_000002.10:g.47887205G>T	NCBI36
NG_007111.1:g.28416G>T , LRG_219:g.28416G>T
NG_008397.1:g.104114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3615G>T (MSH6)	ENSP00000406248.2:p.Arg1205Ser
ENST00000420813.6:c.3615G>T (MSH6)	ENSP00000390382.2:p.Arg1205Ser
ENST00000455383.6:c.3615G>T (MSH6)	ENSP00000397484.2:p.Arg1205Ser
ENST00000700004.2:c.3528G>T (MSH6)	ENSP00000514752.2:p.Arg1176Ser
ENST00000699999.1:n.4586G>T (MSH6)
ENST00000700000.1:c.2346G>T (MSH6)	ENSP00000514749.1:p.Arg782Ser
ENST00000700002.1:c.3918G>T (MSH6)	ENSP00000514750.1:p.Arg1306Ser
ENST00000700003.1:c.1367G>T (MSH6)	ENSP00000514751.1:n.1367G>T
ENST00000700004.1:c.2685G>T (MSH6)	ENSP00000514752.1:p.Arg895Ser
ENST00000700005.1:n.2763G>T (MSH6)
ENST00000700006.1:n.5070G>T (MSH6)
ENST00000700007.1:n.2507G>T (MSH6)
ENST00000700008.1:n.2174G>T (MSH6)
ENST00000700009.1:n.2576G>T (MSH6)
ENST00000700010.1:n.1321G>T (MSH6)
ENST00000700011.1:n.3206G>T (MSH6)
ENST00000682451.1:n.4186C>A (FBXO11)
ENST00000684712.1:n.4448C>A (FBXO11)
ENST00000234420.11:c.3912G>T (MSH6) MANE Select	ENSP00000234420.5:p.Arg1304Ser
ENST00000540021.6:c.3522G>T (MSH6)	ENSP00000446475.1:p.Arg1174Ser
ENST00000652107.1:c.3615G>T (MSH6)	ENSP00000498629.1:p.Arg1205Ser
ENST00000673637.1:c.3615G>T (MSH6)	ENSP00000501310.1:p.Arg1205Ser
ENST00000234420.9:c.3912G>T (MSH6)	ENSP00000234420.4:p.Arg1304Ser
ENST00000405808.5:c.169+1633C>A (FBXO11)	ENSP00000385127.1:n.169+1633C>A
ENST00000434234.5:c.*124+1432C>A (FBXO11)	ENSP00000402692.1:n.*124+1432C>A
ENST00000445503.5:c.*3259G>T (MSH6)	ENSP00000405294.1:n.*3259G>T
ENST00000538136.1:c.3006G>T (MSH6)	ENSP00000438580.1:p.Arg1002Ser
ENST00000540021.5:c.3522G>T (MSH6)	ENSP00000446475.1:p.Arg1174Ser
ENST00000614496.4:c.3006G>T (MSH6)	ENSP00000477844.1:p.Arg1002Ser
ENST00000622629.4:c.813G>T (MSH6)	ENSP00000482078.1:p.Arg271Ser
NM_000179.2:c.3912G>T , LRG_219t1:c.3912G>T (MSH6)	NP_000170.1:p.Arg1304Ser
NM_001281492.1:c.3522G>T (MSH6)	NP_001268421.1:p.Arg1174Ser
NM_001281493.1:c.3006G>T (MSH6)	NP_001268422.1:p.Arg1002Ser
NM_001281494.1:c.3006G>T (MSH6)	NP_001268423.1:p.Arg1002Ser
XM_005264271.1:c.3615G>T (MSH6)	XP_005264328.1:p.Arg1205Ser
XM_011532798.1:c.3729G>T (MSH6)	XP_011531100.1:p.Arg1243Ser
XM_011532799.1:c.3615G>T (MSH6)	XP_011531101.1:p.Arg1205Ser
XM_011532800.1:c.3615G>T (MSH6)	XP_011531102.1:p.Arg1205Ser
XM_024452819.1:c.4005G>T (MSH6)	XP_024308587.1:p.Arg1335Ser
XM_024452820.1:c.3822G>T (MSH6)	XP_024308588.1:p.Arg1274Ser
XM_024452821.1:c.3708G>T (MSH6)	XP_024308589.1:p.Arg1236Ser
XM_024452822.1:c.3099G>T (MSH6)	XP_024308590.1:p.Arg1033Ser
NM_000179.3:c.3912G>T (MSH6) MANE Select	NP_000170.1:p.Arg1304Ser
NM_001281492.2:c.3522G>T (MSH6)	NP_001268421.1:p.Arg1174Ser
NM_001281493.2:c.3006G>T (MSH6)	NP_001268422.1:p.Arg1002Ser
NM_001281494.2:c.3006G>T (MSH6)	NP_001268423.1:p.Arg1002Ser