Canonical Allele Identifier: CA2537448261

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803492_47803493insA , CM000664.2:g.47803492_47803493insA	GRCh38
NC_000002.11:g.48030631_48030632insA , CM000664.1:g.48030631_48030632insA	GRCh37
NC_000002.10:g.47884135_47884136insA	NCBI36
NG_007111.1:g.25346_25347insA , LRG_219:g.25346_25347insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2948_2949insA (MSH6)	ENSP00000406248.2:p.Glu984GlyfsTer10
ENST00000420813.6:c.2948_2949insA (MSH6)	ENSP00000390382.2:p.Glu984GlyfsTer10
ENST00000455383.6:c.2948_2949insA (MSH6)	ENSP00000397484.2:p.Glu984GlyfsTer10
ENST00000700004.2:c.3173-2126_3173-2125insA (MSH6)	ENSP00000514752.2:n.3173-2126_3173-2125insA
ENST00000699999.1:n.3329_3330insA (MSH6)
ENST00000700000.1:c.1679_1680insA (MSH6)	ENSP00000514749.1:p.Glu561GlyfsTer10
ENST00000700002.1:c.3251_3252insA (MSH6)	ENSP00000514750.1:p.Glu1085GlyfsTer10
ENST00000700003.1:c.700_701insA (MSH6)	ENSP00000514751.1:n.700_701insA
ENST00000700004.1:c.2330-2126_2330-2125insA (MSH6)	ENSP00000514752.1:n.2330-2126_2330-2125insA
ENST00000700005.1:n.2096_2097insA (MSH6)
ENST00000700006.1:n.2093_2094insA (MSH6)
ENST00000700007.1:n.1250_1251insA (MSH6)
ENST00000700008.1:n.824_825insA (MSH6)
ENST00000700009.1:n.823_824insA (MSH6)
ENST00000700010.1:n.654_655insA (MSH6)
ENST00000700011.1:n.725_726insA (MSH6)
ENST00000234420.11:c.3245_3246insA (MSH6) MANE Select	ENSP00000234420.5:p.Glu1083GlyfsTer10
ENST00000540021.6:c.2855_2856insA (MSH6)	ENSP00000446475.1:p.Glu953GlyfsTer10
ENST00000652107.1:c.2948_2949insA (MSH6)	ENSP00000498629.1:p.Glu984GlyfsTer10
ENST00000673637.1:c.2948_2949insA (MSH6)	ENSP00000501310.1:p.Glu984GlyfsTer10
ENST00000234420.9:c.3245_3246insA (MSH6)	ENSP00000234420.4:p.Glu1083GlyfsTer10
ENST00000405808.5:c.169+4702_169+4703insT (FBXO11)	ENSP00000385127.1:n.169+4702_169+4703insT
ENST00000434234.5:c.*124+4501_*124+4502insT (FBXO11)	ENSP00000402692.1:n.*124+4501_*124+4502insT
ENST00000445503.5:c.*2592_*2593insA (MSH6)	ENSP00000405294.1:n.*2592_*2593insA
ENST00000538136.1:c.2339_2340insA (MSH6)	ENSP00000438580.1:p.Glu781GlyfsTer10
ENST00000540021.5:c.2855_2856insA (MSH6)	ENSP00000446475.1:p.Glu953GlyfsTer10
ENST00000614496.4:c.2339_2340insA (MSH6)	ENSP00000477844.1:p.Glu781GlyfsTer10
ENST00000622629.4:c.149_150insA (MSH6)	ENSP00000482078.1:p.Glu51GlyfsTer10
NM_000179.2:c.3245_3246insA , LRG_219t1:c.3245_3246insA (MSH6)	NP_000170.1:p.Glu1083GlyfsTer10
NM_001281492.1:c.2855_2856insA (MSH6)	NP_001268421.1:p.Glu953GlyfsTer10
NM_001281493.1:c.2339_2340insA (MSH6)	NP_001268422.1:p.Glu781GlyfsTer10
NM_001281494.1:c.2339_2340insA (MSH6)	NP_001268423.1:p.Glu781GlyfsTer10
XM_005264271.1:c.2948_2949insA (MSH6)	XP_005264328.1:p.Glu984GlyfsTer10
XM_011532798.1:c.3062_3063insA (MSH6)	XP_011531100.1:p.Glu1022GlyfsTer10
XM_011532799.1:c.2948_2949insA (MSH6)	XP_011531101.1:p.Glu984GlyfsTer10
XM_011532800.1:c.2948_2949insA (MSH6)	XP_011531102.1:p.Glu984GlyfsTer10
XM_024452819.1:c.3245_3246insA (MSH6)	XP_024308587.1:p.Glu1083GlyfsTer10
XM_024452820.1:c.3062_3063insA (MSH6)	XP_024308588.1:p.Glu1022GlyfsTer10
XM_024452821.1:c.2948_2949insA (MSH6)	XP_024308589.1:p.Glu984GlyfsTer10
XM_024452822.1:c.2339_2340insA (MSH6)	XP_024308590.1:p.Glu781GlyfsTer10
NM_000179.3:c.3245_3246insA (MSH6) MANE Select	NP_000170.1:p.Glu1083GlyfsTer10
NM_001281492.2:c.2855_2856insA (MSH6)	NP_001268421.1:p.Glu953GlyfsTer10
NM_001281493.2:c.2339_2340insA (MSH6)	NP_001268422.1:p.Glu781GlyfsTer10
NM_001281494.2:c.2339_2340insA (MSH6)	NP_001268423.1:p.Glu781GlyfsTer10