Canonical Allele Identifier: CA2586964940

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804953_47804981del , CM000664.2:g.47804953_47804981del	GRCh38
NC_000002.11:g.48032092_48032120del , CM000664.1:g.48032092_48032120del	GRCh37
NC_000002.10:g.47885596_47885624del	NCBI36
NG_007111.1:g.26807_26835del , LRG_219:g.26807_26835del
NG_008397.1:g.105695_105723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3185_3213del (MSH6)	ENSP00000406248.2:p.Pro1062ArgfsTer2
ENST00000420813.6:c.3185_3213del (MSH6)	ENSP00000390382.2:p.Pro1062ArgfsTer2
ENST00000455383.6:c.3185_3213del (MSH6)	ENSP00000397484.2:p.Pro1062ArgfsTer2
ENST00000700004.2:c.3173-665_3173-637del (MSH6)	ENSP00000514752.2:n.3173-665_3173-637del
ENST00000699999.1:n.3566_3594del (MSH6)
ENST00000700000.1:c.1916_1944del (MSH6)	ENSP00000514749.1:p.Pro639ArgfsTer2
ENST00000700002.1:c.3488_3516del (MSH6)	ENSP00000514750.1:p.Pro1163ArgfsTer2
ENST00000700003.1:c.937_965del (MSH6)	ENSP00000514751.1:n.937_965del
ENST00000700004.1:c.2330-665_2330-637del (MSH6)	ENSP00000514752.1:n.2330-665_2330-637del
ENST00000700005.1:n.2333_2361del (MSH6)
ENST00000700006.1:n.3554_3582del (MSH6)
ENST00000700007.1:n.1487_1515del (MSH6)
ENST00000700008.1:n.1061_1089del (MSH6)
ENST00000700009.1:n.1060_1088del (MSH6)
ENST00000700010.1:n.891_919del (MSH6)
ENST00000700011.1:n.2186_2214del (MSH6)
ENST00000234420.11:c.3482_3510del (MSH6) MANE Select	ENSP00000234420.5:p.Pro1161ArgfsTer2
ENST00000540021.6:c.3092_3120del (MSH6)	ENSP00000446475.1:p.Pro1031ArgfsTer2
ENST00000652107.1:c.3185_3213del (MSH6)	ENSP00000498629.1:p.Pro1062ArgfsTer2
ENST00000673637.1:c.3185_3213del (MSH6)	ENSP00000501310.1:p.Pro1062ArgfsTer2
ENST00000234420.9:c.3482_3510del (MSH6)	ENSP00000234420.4:p.Pro1161ArgfsTer2
ENST00000405808.5:c.169+3214_169+3242del (FBXO11)	ENSP00000385127.1:n.169+3214_169+3242del
ENST00000434234.5:c.*124+3013_*124+3041del (FBXO11)	ENSP00000402692.1:n.*124+3013_*124+3041del
ENST00000445503.5:c.*2829_*2857del (MSH6)	ENSP00000405294.1:n.*2829_*2857del
ENST00000538136.1:c.2576_2604del (MSH6)	ENSP00000438580.1:p.Pro859ArgfsTer2
ENST00000540021.5:c.3092_3120del (MSH6)	ENSP00000446475.1:p.Pro1031ArgfsTer2
ENST00000614496.4:c.2576_2604del (MSH6)	ENSP00000477844.1:p.Pro859ArgfsTer2
ENST00000622629.4:c.386_414del (MSH6)	ENSP00000482078.1:p.Pro129ArgfsTer2
NM_000179.2:c.3482_3510del , LRG_219t1:c.3482_3510del (MSH6)	NP_000170.1:p.Pro1161ArgfsTer2
NM_001281492.1:c.3092_3120del (MSH6)	NP_001268421.1:p.Pro1031ArgfsTer2
NM_001281493.1:c.2576_2604del (MSH6)	NP_001268422.1:p.Pro859ArgfsTer2
NM_001281494.1:c.2576_2604del (MSH6)	NP_001268423.1:p.Pro859ArgfsTer2
XM_005264271.1:c.3185_3213del (MSH6)	XP_005264328.1:p.Pro1062ArgfsTer2
XM_011532798.1:c.3299_3327del (MSH6)	XP_011531100.1:p.Pro1100ArgfsTer2
XM_011532799.1:c.3185_3213del (MSH6)	XP_011531101.1:p.Pro1062ArgfsTer2
XM_011532800.1:c.3185_3213del (MSH6)	XP_011531102.1:p.Pro1062ArgfsTer2
XM_024452819.1:c.3482_3510del (MSH6)	XP_024308587.1:p.Pro1161ArgfsTer2
XM_024452820.1:c.3299_3327del (MSH6)	XP_024308588.1:p.Pro1100ArgfsTer2
XM_024452821.1:c.3185_3213del (MSH6)	XP_024308589.1:p.Pro1062ArgfsTer2
XM_024452822.1:c.2576_2604del (MSH6)	XP_024308590.1:p.Pro859ArgfsTer2
NM_000179.3:c.3482_3510del (MSH6) MANE Select	NP_000170.1:p.Pro1161ArgfsTer2
NM_001281492.2:c.3092_3120del (MSH6)	NP_001268421.1:p.Pro1031ArgfsTer2
NM_001281493.2:c.2576_2604del (MSH6)	NP_001268422.1:p.Pro859ArgfsTer2
NM_001281494.2:c.2576_2604del (MSH6)	NP_001268423.1:p.Pro859ArgfsTer2