Canonical Allele Identifier: CA2496049386

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669454643

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800354_47800355insA , CM000664.2:g.47800354_47800355insA	GRCh38
NC_000002.11:g.48027493_48027494insA , CM000664.1:g.48027493_48027494insA	GRCh37
NC_000002.10:g.47880997_47880998insA	NCBI36
NG_007111.1:g.22208_22209insA , LRG_219:g.22208_22209insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2074_2075insA (MSH6)	ENSP00000406248.2:p.Arg692GlnfsTer13
ENST00000420813.6:c.2074_2075insA (MSH6)	ENSP00000390382.2:p.Arg692GlnfsTer13
ENST00000455383.6:c.2074_2075insA (MSH6)	ENSP00000397484.2:p.Arg692GlnfsTer13
ENST00000700004.2:c.2371_2372insA (MSH6)	ENSP00000514752.2:p.Arg791GlnfsTer13
ENST00000699999.1:n.2455_2456insA (MSH6)
ENST00000700000.1:c.1606+765_1606+766insA (MSH6)	ENSP00000514749.1:n.1606+765_1606+766insA
ENST00000700002.1:c.2377_2378insA (MSH6)	ENSP00000514750.1:p.Arg793GlnfsTer13
ENST00000700003.1:c.628-3066_628-3065insA (MSH6)	ENSP00000514751.1:n.628-3066_628-3065insA
ENST00000700004.1:c.1528_1529insA (MSH6)	ENSP00000514752.1:p.Arg510GlnfsTer13
ENST00000234420.11:c.2371_2372insA (MSH6) MANE Select	ENSP00000234420.5:p.Arg791GlnfsTer13
ENST00000540021.6:c.1981_1982insA (MSH6)	ENSP00000446475.1:p.Arg661GlnfsTer13
ENST00000652107.1:c.2074_2075insA (MSH6)	ENSP00000498629.1:p.Arg692GlnfsTer13
ENST00000673637.1:c.2074_2075insA (MSH6)	ENSP00000501310.1:p.Arg692GlnfsTer13
ENST00000234420.9:c.2371_2372insA (MSH6)	ENSP00000234420.4:p.Arg791GlnfsTer13
ENST00000405808.5:c.169+7840_169+7841insT (FBXO11)	ENSP00000385127.1:n.169+7840_169+7841insT
ENST00000434234.5:c.*124+7639_*124+7640insT (FBXO11)	ENSP00000402692.1:n.*124+7639_*124+7640insT
ENST00000445503.5:c.*1718_*1719insA (MSH6)	ENSP00000405294.1:n.*1718_*1719insA
ENST00000538136.1:c.1465_1466insA (MSH6)	ENSP00000438580.1:p.Arg489GlnfsTer13
ENST00000540021.5:c.1981_1982insA (MSH6)	ENSP00000446475.1:p.Arg661GlnfsTer13
ENST00000614496.4:c.1465_1466insA (MSH6)	ENSP00000477844.1:p.Arg489GlnfsTer13
ENST00000616033.4:c.2368_2369insA (MSH6)	ENSP00000480261.1:p.Arg790GlnfsTer13
ENST00000622629.4:c.-726_-725insA (MSH6)	ENSP00000482078.1:n.-726_-725insA
NM_000179.2:c.2371_2372insA , LRG_219t1:c.2371_2372insA (MSH6)	NP_000170.1:p.Arg791GlnfsTer13
NM_001281492.1:c.1981_1982insA (MSH6)	NP_001268421.1:p.Arg661GlnfsTer13
NM_001281493.1:c.1465_1466insA (MSH6)	NP_001268422.1:p.Arg489GlnfsTer13
NM_001281494.1:c.1465_1466insA (MSH6)	NP_001268423.1:p.Arg489GlnfsTer13
XM_005264271.1:c.2074_2075insA (MSH6)	XP_005264328.1:p.Arg692GlnfsTer13
XM_011532798.1:c.2188_2189insA (MSH6)	XP_011531100.1:p.Arg730GlnfsTer13
XM_011532799.1:c.2074_2075insA (MSH6)	XP_011531101.1:p.Arg692GlnfsTer13
XM_011532800.1:c.2074_2075insA (MSH6)	XP_011531102.1:p.Arg692GlnfsTer13
XM_024452819.1:c.2371_2372insA (MSH6)	XP_024308587.1:p.Arg791GlnfsTer13
XM_024452820.1:c.2188_2189insA (MSH6)	XP_024308588.1:p.Arg730GlnfsTer13
XM_024452821.1:c.2074_2075insA (MSH6)	XP_024308589.1:p.Arg692GlnfsTer13
XM_024452822.1:c.1465_1466insA (MSH6)	XP_024308590.1:p.Arg489GlnfsTer13
NM_000179.3:c.2371_2372insA (MSH6) MANE Select	NP_000170.1:p.Arg791GlnfsTer13
NM_001281492.2:c.1981_1982insA (MSH6)	NP_001268421.1:p.Arg661GlnfsTer13
NM_001281493.2:c.1465_1466insA (MSH6)	NP_001268422.1:p.Arg489GlnfsTer13
NM_001281494.2:c.1465_1466insA (MSH6)	NP_001268423.1:p.Arg489GlnfsTer13