Canonical Allele Identifier: CA2586964943

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804959_47804960del , CM000664.2:g.47804959_47804960del	GRCh38
NC_000002.11:g.48032098_48032099del , CM000664.1:g.48032098_48032099del	GRCh37
NC_000002.10:g.47885602_47885603del	NCBI36
NG_007111.1:g.26813_26814del , LRG_219:g.26813_26814del
NG_008397.1:g.105716_105717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3191_3192del (MSH6)	ENSP00000406248.2:p.Glu1064GlyfsTer8
ENST00000420813.6:c.3191_3192del (MSH6)	ENSP00000390382.2:p.Glu1064GlyfsTer8
ENST00000455383.6:c.3191_3192del (MSH6)	ENSP00000397484.2:p.Glu1064GlyfsTer8
ENST00000700004.2:c.3173-659_3173-658del (MSH6)	ENSP00000514752.2:n.3173-659_3173-658del
ENST00000699999.1:n.3572_3573del (MSH6)
ENST00000700000.1:c.1922_1923del (MSH6)	ENSP00000514749.1:p.Glu641GlyfsTer8
ENST00000700002.1:c.3494_3495del (MSH6)	ENSP00000514750.1:p.Glu1165GlyfsTer8
ENST00000700003.1:c.943_944del (MSH6)	ENSP00000514751.1:n.943_944del
ENST00000700004.1:c.2330-659_2330-658del (MSH6)	ENSP00000514752.1:n.2330-659_2330-658del
ENST00000700005.1:n.2339_2340del (MSH6)
ENST00000700006.1:n.3560_3561del (MSH6)
ENST00000700007.1:n.1493_1494del (MSH6)
ENST00000700008.1:n.1067_1068del (MSH6)
ENST00000700009.1:n.1066_1067del (MSH6)
ENST00000700010.1:n.897_898del (MSH6)
ENST00000700011.1:n.2192_2193del (MSH6)
ENST00000234420.11:c.3488_3489del (MSH6) MANE Select	ENSP00000234420.5:p.Glu1163GlyfsTer8
ENST00000540021.6:c.3098_3099del (MSH6)	ENSP00000446475.1:p.Glu1033GlyfsTer8
ENST00000652107.1:c.3191_3192del (MSH6)	ENSP00000498629.1:p.Glu1064GlyfsTer8
ENST00000673637.1:c.3191_3192del (MSH6)	ENSP00000501310.1:p.Glu1064GlyfsTer8
ENST00000234420.9:c.3488_3489del (MSH6)	ENSP00000234420.4:p.Glu1163GlyfsTer8
ENST00000405808.5:c.169+3235_169+3236del (FBXO11)	ENSP00000385127.1:n.169+3235_169+3236del
ENST00000434234.5:c.*124+3034_*124+3035del (FBXO11)	ENSP00000402692.1:n.*124+3034_*124+3035del
ENST00000445503.5:c.*2835_*2836del (MSH6)	ENSP00000405294.1:n.*2835_*2836del
ENST00000538136.1:c.2582_2583del (MSH6)	ENSP00000438580.1:p.Glu861GlyfsTer8
ENST00000540021.5:c.3098_3099del (MSH6)	ENSP00000446475.1:p.Glu1033GlyfsTer8
ENST00000614496.4:c.2582_2583del (MSH6)	ENSP00000477844.1:p.Glu861GlyfsTer8
ENST00000622629.4:c.392_393del (MSH6)	ENSP00000482078.1:p.Glu131GlyfsTer8
NM_000179.2:c.3488_3489del , LRG_219t1:c.3488_3489del (MSH6)	NP_000170.1:p.Glu1163GlyfsTer8
NM_001281492.1:c.3098_3099del (MSH6)	NP_001268421.1:p.Glu1033GlyfsTer8
NM_001281493.1:c.2582_2583del (MSH6)	NP_001268422.1:p.Glu861GlyfsTer8
NM_001281494.1:c.2582_2583del (MSH6)	NP_001268423.1:p.Glu861GlyfsTer8
XM_005264271.1:c.3191_3192del (MSH6)	XP_005264328.1:p.Glu1064GlyfsTer8
XM_011532798.1:c.3305_3306del (MSH6)	XP_011531100.1:p.Glu1102GlyfsTer8
XM_011532799.1:c.3191_3192del (MSH6)	XP_011531101.1:p.Glu1064GlyfsTer8
XM_011532800.1:c.3191_3192del (MSH6)	XP_011531102.1:p.Glu1064GlyfsTer8
XM_024452819.1:c.3488_3489del (MSH6)	XP_024308587.1:p.Glu1163GlyfsTer8
XM_024452820.1:c.3305_3306del (MSH6)	XP_024308588.1:p.Glu1102GlyfsTer8
XM_024452821.1:c.3191_3192del (MSH6)	XP_024308589.1:p.Glu1064GlyfsTer8
XM_024452822.1:c.2582_2583del (MSH6)	XP_024308590.1:p.Glu861GlyfsTer8
NM_000179.3:c.3488_3489del (MSH6) MANE Select	NP_000170.1:p.Glu1163GlyfsTer8
NM_001281492.2:c.3098_3099del (MSH6)	NP_001268421.1:p.Glu1033GlyfsTer8
NM_001281493.2:c.2582_2583del (MSH6)	NP_001268422.1:p.Glu861GlyfsTer8
NM_001281494.2:c.2582_2583del (MSH6)	NP_001268423.1:p.Glu861GlyfsTer8