Canonical Allele Identifier: CA2496054173

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806315_47806318delinsTAGA , CM000664.2:g.47806315_47806318delinsTAGA	GRCh38
NC_000002.11:g.48033454_48033457delinsTAGA , CM000664.1:g.48033454_48033457delinsTAGA	GRCh37
NC_000002.10:g.47886958_47886961delinsTAGA	NCBI36
NG_007111.1:g.28169_28172delinsTAGA , LRG_219:g.28169_28172delinsTAGA
NG_008397.1:g.104358_104361delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3461_3464delinsTAGA (MSH6)	ENSP00000406248.2:p.Val1154=
ENST00000420813.6:c.3461_3464delinsTAGA (MSH6)	ENSP00000390382.2:p.Val1154=
ENST00000455383.6:c.3461_3464delinsTAGA (MSH6)	ENSP00000397484.2:p.Val1154=
ENST00000700004.2:c.3374_3377delinsTAGA (MSH6)	ENSP00000514752.2:p.Val1125=
ENST00000699999.1:n.4432_4435delinsTAGA (MSH6)
ENST00000700000.1:c.2192_2195delinsTAGA (MSH6)	ENSP00000514749.1:p.Val731=
ENST00000700002.1:c.3764_3767delinsTAGA (MSH6)	ENSP00000514750.1:p.Val1255=
ENST00000700003.1:c.1213_1216delinsTAGA (MSH6)	ENSP00000514751.1:n.1213_1216delinsTAGA
ENST00000700004.1:c.2531_2534delinsTAGA (MSH6)	ENSP00000514752.1:p.Val844=
ENST00000700005.1:n.2609_2612delinsTAGA (MSH6)
ENST00000700006.1:n.4916_4919delinsTAGA (MSH6)
ENST00000700007.1:n.2353_2356delinsTAGA (MSH6)
ENST00000700008.1:n.1927_1930delinsTAGA (MSH6)
ENST00000700009.1:n.2422_2425delinsTAGA (MSH6)
ENST00000700010.1:n.1167_1170delinsTAGA (MSH6)
ENST00000700011.1:n.3052_3055delinsTAGA (MSH6)
ENST00000682451.1:n.4430_4433delinsTCTA (FBXO11)
ENST00000684712.1:n.4692_4695delinsTCTA (FBXO11)
ENST00000234420.11:c.3758_3761delinsTAGA (MSH6) MANE Select	ENSP00000234420.5:p.Val1253=
ENST00000540021.6:c.3368_3371delinsTAGA (MSH6)	ENSP00000446475.1:p.Val1123=
ENST00000652107.1:c.3461_3464delinsTAGA (MSH6)	ENSP00000498629.1:p.Val1154=
ENST00000673637.1:c.3461_3464delinsTAGA (MSH6)	ENSP00000501310.1:p.Val1154=
ENST00000234420.9:c.3758_3761delinsTAGA (MSH6)	ENSP00000234420.4:p.Val1253=
ENST00000405808.5:c.169+1877_169+1880delinsTCTA (FBXO11)	ENSP00000385127.1:n.169+1877_169+1880delinsTCTA
ENST00000434234.5:c.*124+1676_*124+1679delinsTCTA (FBXO11)	ENSP00000402692.1:n.*124+1676_*124+1679delinsTCTA
ENST00000445503.5:c.*3105_*3108delinsTAGA (MSH6)	ENSP00000405294.1:n.*3105_*3108delinsTAGA
ENST00000538136.1:c.2852_2855delinsTAGA (MSH6)	ENSP00000438580.1:p.Val951=
ENST00000540021.5:c.3368_3371delinsTAGA (MSH6)	ENSP00000446475.1:p.Val1123=
ENST00000614496.4:c.2852_2855delinsTAGA (MSH6)	ENSP00000477844.1:p.Val951=
ENST00000622629.4:c.660_663delinsTAGA (MSH6)	ENSP00000482078.1:p.Ser220=
NM_000179.2:c.3758_3761delinsTAGA , LRG_219t1:c.3758_3761delinsTAGA (MSH6)	NP_000170.1:p.Val1253=
NM_001281492.1:c.3368_3371delinsTAGA (MSH6)	NP_001268421.1:p.Val1123=
NM_001281493.1:c.2852_2855delinsTAGA (MSH6)	NP_001268422.1:p.Val951=
NM_001281494.1:c.2852_2855delinsTAGA (MSH6)	NP_001268423.1:p.Val951=
XM_005264271.1:c.3461_3464delinsTAGA (MSH6)	XP_005264328.1:p.Val1154=
XM_011532798.1:c.3575_3578delinsTAGA (MSH6)	XP_011531100.1:p.Val1192=
XM_011532799.1:c.3461_3464delinsTAGA (MSH6)	XP_011531101.1:p.Val1154=
XM_011532800.1:c.3461_3464delinsTAGA (MSH6)	XP_011531102.1:p.Val1154=
XM_024452819.1:c.3758_3761delinsTAGA (MSH6)	XP_024308587.1:p.Val1253=
XM_024452820.1:c.3575_3578delinsTAGA (MSH6)	XP_024308588.1:p.Val1192=
XM_024452821.1:c.3461_3464delinsTAGA (MSH6)	XP_024308589.1:p.Val1154=
XM_024452822.1:c.2852_2855delinsTAGA (MSH6)	XP_024308590.1:p.Val951=
NM_000179.3:c.3758_3761delinsTAGA (MSH6) MANE Select	NP_000170.1:p.Val1253=
NM_001281492.2:c.3368_3371delinsTAGA (MSH6)	NP_001268421.1:p.Val1123=
NM_001281493.2:c.2852_2855delinsTAGA (MSH6)	NP_001268422.1:p.Val951=
NM_001281494.2:c.2852_2855delinsTAGA (MSH6)	NP_001268423.1:p.Val951=