Canonical Allele Identifier: CA2496051834

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803483_47803485delinsTTC , CM000664.2:g.47803483_47803485delinsTTC	GRCh38
NC_000002.11:g.48030622_48030624delinsTTC , CM000664.1:g.48030622_48030624delinsTTC	GRCh37
NC_000002.10:g.47884126_47884128delinsTTC	NCBI36
NG_007111.1:g.25337_25339delinsTTC , LRG_219:g.25337_25339delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2939_2941delinsTTC (MSH6)	ENSP00000406248.2:p.Ile980=
ENST00000420813.6:c.2939_2941delinsTTC (MSH6)	ENSP00000390382.2:p.Ile980=
ENST00000455383.6:c.2939_2941delinsTTC (MSH6)	ENSP00000397484.2:p.Ile980=
ENST00000700004.2:c.3173-2135_3173-2133delinsTTC (MSH6)	ENSP00000514752.2:n.3173-2135_3173-2133delinsTTC
ENST00000699999.1:n.3320_3322delinsTTC (MSH6)
ENST00000700000.1:c.1670_1672delinsTTC (MSH6)	ENSP00000514749.1:p.Ile557=
ENST00000700002.1:c.3242_3244delinsTTC (MSH6)	ENSP00000514750.1:p.Ile1081=
ENST00000700003.1:c.691_693delinsTTC (MSH6)	ENSP00000514751.1:n.691_693delinsTTC
ENST00000700004.1:c.2330-2135_2330-2133delinsTTC (MSH6)	ENSP00000514752.1:n.2330-2135_2330-2133delinsTTC
ENST00000700005.1:n.2087_2089delinsTTC (MSH6)
ENST00000700006.1:n.2084_2086delinsTTC (MSH6)
ENST00000700007.1:n.1241_1243delinsTTC (MSH6)
ENST00000700008.1:n.815_817delinsTTC (MSH6)
ENST00000700009.1:n.814_816delinsTTC (MSH6)
ENST00000700010.1:n.645_647delinsTTC (MSH6)
ENST00000700011.1:n.716_718delinsTTC (MSH6)
ENST00000234420.11:c.3236_3238delinsTTC (MSH6) MANE Select	ENSP00000234420.5:p.Ile1079=
ENST00000540021.6:c.2846_2848delinsTTC (MSH6)	ENSP00000446475.1:p.Ile949=
ENST00000652107.1:c.2939_2941delinsTTC (MSH6)	ENSP00000498629.1:p.Ile980=
ENST00000673637.1:c.2939_2941delinsTTC (MSH6)	ENSP00000501310.1:p.Ile980=
ENST00000234420.9:c.3236_3238delinsTTC (MSH6)	ENSP00000234420.4:p.Ile1079=
ENST00000405808.5:c.169+4710_169+4712delinsGAA (FBXO11)	ENSP00000385127.1:n.169+4710_169+4712delinsGAA
ENST00000434234.5:c.*124+4509_*124+4511delinsGAA (FBXO11)	ENSP00000402692.1:n.*124+4509_*124+4511delinsGAA
ENST00000445503.5:c.*2583_*2585delinsTTC (MSH6)	ENSP00000405294.1:n.*2583_*2585delinsTTC
ENST00000538136.1:c.2330_2332delinsTTC (MSH6)	ENSP00000438580.1:p.Ile777=
ENST00000540021.5:c.2846_2848delinsTTC (MSH6)	ENSP00000446475.1:p.Ile949=
ENST00000614496.4:c.2330_2332delinsTTC (MSH6)	ENSP00000477844.1:p.Ile777=
ENST00000622629.4:c.140_142delinsTTC (MSH6)	ENSP00000482078.1:p.Ile47=
NM_000179.2:c.3236_3238delinsTTC , LRG_219t1:c.3236_3238delinsTTC (MSH6)	NP_000170.1:p.Ile1079=
NM_001281492.1:c.2846_2848delinsTTC (MSH6)	NP_001268421.1:p.Ile949=
NM_001281493.1:c.2330_2332delinsTTC (MSH6)	NP_001268422.1:p.Ile777=
NM_001281494.1:c.2330_2332delinsTTC (MSH6)	NP_001268423.1:p.Ile777=
XM_005264271.1:c.2939_2941delinsTTC (MSH6)	XP_005264328.1:p.Ile980=
XM_011532798.1:c.3053_3055delinsTTC (MSH6)	XP_011531100.1:p.Ile1018=
XM_011532799.1:c.2939_2941delinsTTC (MSH6)	XP_011531101.1:p.Ile980=
XM_011532800.1:c.2939_2941delinsTTC (MSH6)	XP_011531102.1:p.Ile980=
XM_024452819.1:c.3236_3238delinsTTC (MSH6)	XP_024308587.1:p.Ile1079=
XM_024452820.1:c.3053_3055delinsTTC (MSH6)	XP_024308588.1:p.Ile1018=
XM_024452821.1:c.2939_2941delinsTTC (MSH6)	XP_024308589.1:p.Ile980=
XM_024452822.1:c.2330_2332delinsTTC (MSH6)	XP_024308590.1:p.Ile777=
NM_000179.3:c.3236_3238delinsTTC (MSH6) MANE Select	NP_000170.1:p.Ile1079=
NM_001281492.2:c.2846_2848delinsTTC (MSH6)	NP_001268421.1:p.Ile949=
NM_001281493.2:c.2330_2332delinsTTC (MSH6)	NP_001268422.1:p.Ile777=
NM_001281494.2:c.2330_2332delinsTTC (MSH6)	NP_001268423.1:p.Ile777=