Canonical Allele Identifier: CA2496054557

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806803_47806805delinsGTC , CM000664.2:g.47806803_47806805delinsGTC	GRCh38
NC_000002.11:g.48033942_48033944delinsGTC , CM000664.1:g.48033942_48033944delinsGTC	GRCh37
NC_000002.10:g.47887446_47887448delinsGTC	NCBI36
NG_007111.1:g.28657_28659delinsGTC , LRG_219:g.28657_28659delinsGTC
NG_008397.1:g.103871_103873delinsGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3729_3731delinsGTC (MSH6)	ENSP00000406248.2:p.Arg1243=
ENST00000420813.6:c.3729_3731delinsGTC (MSH6)	ENSP00000390382.2:p.Arg1243=
ENST00000455383.6:c.3729_3731delinsGTC (MSH6)	ENSP00000397484.2:p.Arg1243=
ENST00000700004.2:c.3642_3644delinsGTC (MSH6)	ENSP00000514752.2:p.Arg1214=
ENST00000699999.1:n.4700_4702delinsGTC (MSH6)
ENST00000700000.1:c.2460_2462delinsGTC (MSH6)	ENSP00000514749.1:p.Arg820=
ENST00000700002.1:c.4032_4034delinsGTC (MSH6)	ENSP00000514750.1:p.Arg1344=
ENST00000700003.1:c.1481_1483delinsGTC (MSH6)	ENSP00000514751.1:n.1481_1483delinsGTC
ENST00000700004.1:c.2799_2801delinsGTC (MSH6)	ENSP00000514752.1:p.Arg933=
ENST00000700005.1:n.3004_3006delinsGTC (MSH6)
ENST00000700007.1:n.2621_2623delinsGTC (MSH6)
ENST00000700008.1:n.2288_2290delinsGTC (MSH6)
ENST00000700009.1:n.2690_2692delinsGTC (MSH6)
ENST00000700010.1:n.1435_1437delinsGTC (MSH6)
ENST00000700011.1:n.3320_3322delinsGTC (MSH6)
ENST00000682451.1:n.3943_3945delinsGAC (FBXO11)
ENST00000684712.1:n.4205_4207delinsGAC (FBXO11)
ENST00000234420.11:c.4026_4028delinsGTC (MSH6) MANE Select	ENSP00000234420.5:p.Arg1342=
ENST00000540021.6:c.3636_3638delinsGTC (MSH6)	ENSP00000446475.1:p.Arg1212=
ENST00000652107.1:c.3729_3731delinsGTC (MSH6)	ENSP00000498629.1:p.Arg1243=
ENST00000673637.1:c.3729_3731delinsGTC (MSH6)	ENSP00000501310.1:p.Arg1243=
ENST00000234420.9:c.4026_4028delinsGTC (MSH6)	ENSP00000234420.4:p.Arg1342=
ENST00000405808.5:c.169+1390_169+1392delinsGAC (FBXO11)	ENSP00000385127.1:n.169+1390_169+1392delinsGAC
ENST00000434234.5:c.*124+1189_*124+1191delinsGAC (FBXO11)	ENSP00000402692.1:n.*124+1189_*124+1191delinsGAC
ENST00000445503.5:c.*3373_*3375delinsGTC (MSH6)	ENSP00000405294.1:n.*3373_*3375delinsGTC
ENST00000465204.5:n.3105_3107delinsGAC (FBXO11)
ENST00000538136.1:c.3120_3122delinsGTC (MSH6)	ENSP00000438580.1:p.Arg1040=
ENST00000540021.5:c.3636_3638delinsGTC (MSH6)	ENSP00000446475.1:p.Arg1212=
ENST00000614496.4:c.3120_3122delinsGTC (MSH6)	ENSP00000477844.1:p.Arg1040=
ENST00000622629.4:c.927_929delinsGTC (MSH6)	ENSP00000482078.1:p.Arg309=
NM_000179.2:c.4026_4028delinsGTC , LRG_219t1:c.4026_4028delinsGTC (MSH6)	NP_000170.1:p.Arg1342=
NM_001281492.1:c.3636_3638delinsGTC (MSH6)	NP_001268421.1:p.Arg1212=
NM_001281493.1:c.3120_3122delinsGTC (MSH6)	NP_001268422.1:p.Arg1040=
NM_001281494.1:c.3120_3122delinsGTC (MSH6)	NP_001268423.1:p.Arg1040=
XM_005264271.1:c.3729_3731delinsGTC (MSH6)	XP_005264328.1:p.Arg1243=
XM_011532798.1:c.3843_3845delinsGTC (MSH6)	XP_011531100.1:p.Arg1281=
XM_011532799.1:c.3729_3731delinsGTC (MSH6)	XP_011531101.1:p.Arg1243=
XM_011532800.1:c.3729_3731delinsGTC (MSH6)	XP_011531102.1:p.Arg1243=
XM_024452819.1:c.4119_4121delinsGTC (MSH6)	XP_024308587.1:p.Arg1373=
XM_024452820.1:c.3936_3938delinsGTC (MSH6)	XP_024308588.1:p.Arg1312=
XM_024452821.1:c.3822_3824delinsGTC (MSH6)	XP_024308589.1:p.Arg1274=
XM_024452822.1:c.3213_3215delinsGTC (MSH6)	XP_024308590.1:p.Arg1071=
NM_000179.3:c.4026_4028delinsGTC (MSH6) MANE Select	NP_000170.1:p.Arg1342=
NM_001281492.2:c.3636_3638delinsGTC (MSH6)	NP_001268421.1:p.Arg1212=
NM_001281493.2:c.3120_3122delinsGTC (MSH6)	NP_001268422.1:p.Arg1040=
NM_001281494.2:c.3120_3122delinsGTC (MSH6)	NP_001268423.1:p.Arg1040=