Canonical Allele Identifier: CA2496051815

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803465_47803467delinsCTA , CM000664.2:g.47803465_47803467delinsCTA	GRCh38
NC_000002.11:g.48030604_48030606delinsCTA , CM000664.1:g.48030604_48030606delinsCTA	GRCh37
NC_000002.10:g.47884108_47884110delinsCTA	NCBI36
NG_007111.1:g.25319_25321delinsCTA , LRG_219:g.25319_25321delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2921_2923delinsCTA (MSH6)	ENSP00000406248.2:p.Pro974=
ENST00000420813.6:c.2921_2923delinsCTA (MSH6)	ENSP00000390382.2:p.Pro974=
ENST00000455383.6:c.2921_2923delinsCTA (MSH6)	ENSP00000397484.2:p.Pro974=
ENST00000700004.2:c.3173-2153_3173-2151delinsCTA (MSH6)	ENSP00000514752.2:n.3173-2153_3173-2151delinsCTA
ENST00000699999.1:n.3302_3304delinsCTA (MSH6)
ENST00000700000.1:c.1652_1654delinsCTA (MSH6)	ENSP00000514749.1:p.Pro551=
ENST00000700002.1:c.3224_3226delinsCTA (MSH6)	ENSP00000514750.1:p.Pro1075=
ENST00000700003.1:c.673_675delinsCTA (MSH6)	ENSP00000514751.1:p.Leu225=
ENST00000700004.1:c.2330-2153_2330-2151delinsCTA (MSH6)	ENSP00000514752.1:n.2330-2153_2330-2151delinsCTA
ENST00000700005.1:n.2069_2071delinsCTA (MSH6)
ENST00000700006.1:n.2066_2068delinsCTA (MSH6)
ENST00000700007.1:n.1223_1225delinsCTA (MSH6)
ENST00000700008.1:n.797_799delinsCTA (MSH6)
ENST00000700009.1:n.796_798delinsCTA (MSH6)
ENST00000700010.1:n.627_629delinsCTA (MSH6)
ENST00000700011.1:n.698_700delinsCTA (MSH6)
ENST00000234420.11:c.3218_3220delinsCTA (MSH6) MANE Select	ENSP00000234420.5:p.Pro1073=
ENST00000540021.6:c.2828_2830delinsCTA (MSH6)	ENSP00000446475.1:p.Pro943=
ENST00000652107.1:c.2921_2923delinsCTA (MSH6)	ENSP00000498629.1:p.Pro974=
ENST00000673637.1:c.2921_2923delinsCTA (MSH6)	ENSP00000501310.1:p.Pro974=
ENST00000234420.9:c.3218_3220delinsCTA (MSH6)	ENSP00000234420.4:p.Pro1073=
ENST00000405808.5:c.169+4728_169+4730delinsTAG (FBXO11)	ENSP00000385127.1:n.169+4728_169+4730delinsTAG
ENST00000434234.5:c.*124+4527_*124+4529delinsTAG (FBXO11)	ENSP00000402692.1:n.*124+4527_*124+4529delinsTAG
ENST00000445503.5:c.*2565_*2567delinsCTA (MSH6)	ENSP00000405294.1:n.*2565_*2567delinsCTA
ENST00000538136.1:c.2312_2314delinsCTA (MSH6)	ENSP00000438580.1:p.Pro771=
ENST00000540021.5:c.2828_2830delinsCTA (MSH6)	ENSP00000446475.1:p.Pro943=
ENST00000614496.4:c.2312_2314delinsCTA (MSH6)	ENSP00000477844.1:p.Pro771=
ENST00000622629.4:c.122_124delinsCTA (MSH6)	ENSP00000482078.1:p.Pro41=
NM_000179.2:c.3218_3220delinsCTA , LRG_219t1:c.3218_3220delinsCTA (MSH6)	NP_000170.1:p.Pro1073=
NM_001281492.1:c.2828_2830delinsCTA (MSH6)	NP_001268421.1:p.Pro943=
NM_001281493.1:c.2312_2314delinsCTA (MSH6)	NP_001268422.1:p.Pro771=
NM_001281494.1:c.2312_2314delinsCTA (MSH6)	NP_001268423.1:p.Pro771=
XM_005264271.1:c.2921_2923delinsCTA (MSH6)	XP_005264328.1:p.Pro974=
XM_011532798.1:c.3035_3037delinsCTA (MSH6)	XP_011531100.1:p.Pro1012=
XM_011532799.1:c.2921_2923delinsCTA (MSH6)	XP_011531101.1:p.Pro974=
XM_011532800.1:c.2921_2923delinsCTA (MSH6)	XP_011531102.1:p.Pro974=
XM_024452819.1:c.3218_3220delinsCTA (MSH6)	XP_024308587.1:p.Pro1073=
XM_024452820.1:c.3035_3037delinsCTA (MSH6)	XP_024308588.1:p.Pro1012=
XM_024452821.1:c.2921_2923delinsCTA (MSH6)	XP_024308589.1:p.Pro974=
XM_024452822.1:c.2312_2314delinsCTA (MSH6)	XP_024308590.1:p.Pro771=
NM_000179.3:c.3218_3220delinsCTA (MSH6) MANE Select	NP_000170.1:p.Pro1073=
NM_001281492.2:c.2828_2830delinsCTA (MSH6)	NP_001268421.1:p.Pro943=
NM_001281493.2:c.2312_2314delinsCTA (MSH6)	NP_001268422.1:p.Pro771=
NM_001281494.2:c.2312_2314delinsCTA (MSH6)	NP_001268423.1:p.Pro771=