Canonical Allele Identifier: CA2496054062

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806253_47806257delinsTAAAG , CM000664.2:g.47806253_47806257delinsTAAAG	GRCh38
NC_000002.11:g.48033392_48033396delinsTAAAG , CM000664.1:g.48033392_48033396delinsTAAAG	GRCh37
NC_000002.10:g.47886896_47886900delinsTAAAG	NCBI36
NG_007111.1:g.28107_28111delinsTAAAG , LRG_219:g.28107_28111delinsTAAAG
NG_008397.1:g.104419_104423delinsCTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3399_3403delinsTAAAG (MSH6)	ENSP00000406248.2:p.Val1133=
ENST00000420813.6:c.3399_3403delinsTAAAG (MSH6)	ENSP00000390382.2:p.Val1133=
ENST00000455383.6:c.3399_3403delinsTAAAG (MSH6)	ENSP00000397484.2:p.Val1133=
ENST00000700004.2:c.3312_3316delinsTAAAG (MSH6)	ENSP00000514752.2:p.Val1104=
ENST00000699999.1:n.4370_4374delinsTAAAG (MSH6)
ENST00000700000.1:c.2130_2134delinsTAAAG (MSH6)	ENSP00000514749.1:p.Val710=
ENST00000700002.1:c.3702_3706delinsTAAAG (MSH6)	ENSP00000514750.1:p.Val1234=
ENST00000700003.1:c.1151_1155delinsTAAAG (MSH6)	ENSP00000514751.1:n.1151_1155delinsTAAAG
ENST00000700004.1:c.2469_2473delinsTAAAG (MSH6)	ENSP00000514752.1:p.Val823=
ENST00000700005.1:n.2547_2551delinsTAAAG (MSH6)
ENST00000700006.1:n.4854_4858delinsTAAAG (MSH6)
ENST00000700007.1:n.2291_2295delinsTAAAG (MSH6)
ENST00000700008.1:n.1865_1869delinsTAAAG (MSH6)
ENST00000700009.1:n.2360_2364delinsTAAAG (MSH6)
ENST00000700010.1:n.1105_1109delinsTAAAG (MSH6)
ENST00000700011.1:n.2990_2994delinsTAAAG (MSH6)
ENST00000682451.1:n.4491_4495delinsCTTTA (FBXO11)
ENST00000684712.1:n.4753_4757delinsCTTTA (FBXO11)
ENST00000234420.11:c.3696_3700delinsTAAAG (MSH6) MANE Select	ENSP00000234420.5:p.Val1232=
ENST00000540021.6:c.3306_3310delinsTAAAG (MSH6)	ENSP00000446475.1:p.Val1102=
ENST00000652107.1:c.3399_3403delinsTAAAG (MSH6)	ENSP00000498629.1:p.Val1133=
ENST00000673637.1:c.3399_3403delinsTAAAG (MSH6)	ENSP00000501310.1:p.Val1133=
ENST00000234420.9:c.3696_3700delinsTAAAG (MSH6)	ENSP00000234420.4:p.Val1232=
ENST00000405808.5:c.169+1938_169+1942delinsCTTTA (FBXO11)	ENSP00000385127.1:n.169+1938_169+1942deli...
ENST00000434234.5:c.*124+1737_*124+1741delinsCTTTA (FBXO11)	ENSP00000402692.1:n.*124+1737_*124+1741de...
ENST00000445503.5:c.*3043_*3047delinsTAAAG (MSH6)	ENSP00000405294.1:n.*3043_*3047delinsTAAA...
ENST00000538136.1:c.2790_2794delinsTAAAG (MSH6)	ENSP00000438580.1:p.Val930=
ENST00000540021.5:c.3306_3310delinsTAAAG (MSH6)	ENSP00000446475.1:p.Val1102=
ENST00000614496.4:c.2790_2794delinsTAAAG (MSH6)	ENSP00000477844.1:p.Val930=
ENST00000622629.4:c.600_604delinsTAAAG (MSH6)	ENSP00000482078.1:p.Val200=
NM_000179.2:c.3696_3700delinsTAAAG , LRG_219t1:c.3696_3700delinsTAAAG (MSH6)	NP_000170.1:p.Val1232=
NM_001281492.1:c.3306_3310delinsTAAAG (MSH6)	NP_001268421.1:p.Val1102=
NM_001281493.1:c.2790_2794delinsTAAAG (MSH6)	NP_001268422.1:p.Val930=
NM_001281494.1:c.2790_2794delinsTAAAG (MSH6)	NP_001268423.1:p.Val930=
XM_005264271.1:c.3399_3403delinsTAAAG (MSH6)	XP_005264328.1:p.Val1133=
XM_011532798.1:c.3513_3517delinsTAAAG (MSH6)	XP_011531100.1:p.Val1171=
XM_011532799.1:c.3399_3403delinsTAAAG (MSH6)	XP_011531101.1:p.Val1133=
XM_011532800.1:c.3399_3403delinsTAAAG (MSH6)	XP_011531102.1:p.Val1133=
XM_024452819.1:c.3696_3700delinsTAAAG (MSH6)	XP_024308587.1:p.Val1232=
XM_024452820.1:c.3513_3517delinsTAAAG (MSH6)	XP_024308588.1:p.Val1171=
XM_024452821.1:c.3399_3403delinsTAAAG (MSH6)	XP_024308589.1:p.Val1133=
XM_024452822.1:c.2790_2794delinsTAAAG (MSH6)	XP_024308590.1:p.Val930=
NM_000179.3:c.3696_3700delinsTAAAG (MSH6) MANE Select	NP_000170.1:p.Val1232=
NM_001281492.2:c.3306_3310delinsTAAAG (MSH6)	NP_001268421.1:p.Val1102=
NM_001281493.2:c.2790_2794delinsTAAAG (MSH6)	NP_001268422.1:p.Val930=
NM_001281494.2:c.2790_2794delinsTAAAG (MSH6)	NP_001268423.1:p.Val930=