Canonical Allele Identifier: CA2496049505

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800246_47800247delinsGA , CM000664.2:g.47800246_47800247delinsGA	GRCh38
NC_000002.11:g.48027385_48027386delinsGA , CM000664.1:g.48027385_48027386delinsGA	GRCh37
NC_000002.10:g.47880889_47880890delinsGA	NCBI36
NG_007111.1:g.22100_22101delinsGA , LRG_219:g.22100_22101delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1966_1967delinsGA (MSH6)	ENSP00000406248.2:p.Glu656=
ENST00000420813.6:c.1966_1967delinsGA (MSH6)	ENSP00000390382.2:p.Glu656=
ENST00000455383.6:c.1966_1967delinsGA (MSH6)	ENSP00000397484.2:p.Glu656=
ENST00000700004.2:c.2263_2264delinsGA (MSH6)	ENSP00000514752.2:p.Glu755=
ENST00000699999.1:n.2347_2348delinsGA (MSH6)
ENST00000700000.1:c.1606+657_1606+658delinsGA (MSH6)	ENSP00000514749.1:n.1606+657_1606+658delinsGA
ENST00000700002.1:c.2269_2270delinsGA (MSH6)	ENSP00000514750.1:p.Glu757=
ENST00000700003.1:c.628-3174_628-3173delinsGA (MSH6)	ENSP00000514751.1:n.628-3174_628-3173delinsGA
ENST00000700004.1:c.1420_1421delinsGA (MSH6)	ENSP00000514752.1:p.Glu474=
ENST00000234420.11:c.2263_2264delinsGA (MSH6) MANE Select	ENSP00000234420.5:p.Glu755=
ENST00000540021.6:c.1873_1874delinsGA (MSH6)	ENSP00000446475.1:p.Glu625=
ENST00000652107.1:c.1966_1967delinsGA (MSH6)	ENSP00000498629.1:p.Glu656=
ENST00000673637.1:c.1966_1967delinsGA (MSH6)	ENSP00000501310.1:p.Glu656=
ENST00000234420.9:c.2263_2264delinsGA (MSH6)	ENSP00000234420.4:p.Glu755=
ENST00000405808.5:c.169+7948_169+7949delinsTC (FBXO11)	ENSP00000385127.1:n.169+7948_169+7949delinsTC
ENST00000434234.5:c.*124+7747_*124+7748delinsTC (FBXO11)	ENSP00000402692.1:n.*124+7747_*124+7748delinsTC
ENST00000445503.5:c.*1610_*1611delinsGA (MSH6)	ENSP00000405294.1:n.*1610_*1611delinsGA
ENST00000538136.1:c.1357_1358delinsGA (MSH6)	ENSP00000438580.1:p.Glu453=
ENST00000540021.5:c.1873_1874delinsGA (MSH6)	ENSP00000446475.1:p.Glu625=
ENST00000614496.4:c.1357_1358delinsGA (MSH6)	ENSP00000477844.1:p.Glu453=
ENST00000616033.4:c.2260_2261delinsGA (MSH6)	ENSP00000480261.1:p.Glu754=
ENST00000622629.4:c.-834_-833delinsGA (MSH6)	ENSP00000482078.1:n.-834_-833delinsGA
NM_000179.2:c.2263_2264delinsGA , LRG_219t1:c.2263_2264delinsGA (MSH6)	NP_000170.1:p.Glu755=
NM_001281492.1:c.1873_1874delinsGA (MSH6)	NP_001268421.1:p.Glu625=
NM_001281493.1:c.1357_1358delinsGA (MSH6)	NP_001268422.1:p.Glu453=
NM_001281494.1:c.1357_1358delinsGA (MSH6)	NP_001268423.1:p.Glu453=
XM_005264271.1:c.1966_1967delinsGA (MSH6)	XP_005264328.1:p.Glu656=
XM_011532798.1:c.2080_2081delinsGA (MSH6)	XP_011531100.1:p.Glu694=
XM_011532799.1:c.1966_1967delinsGA (MSH6)	XP_011531101.1:p.Glu656=
XM_011532800.1:c.1966_1967delinsGA (MSH6)	XP_011531102.1:p.Glu656=
XM_024452819.1:c.2263_2264delinsGA (MSH6)	XP_024308587.1:p.Glu755=
XM_024452820.1:c.2080_2081delinsGA (MSH6)	XP_024308588.1:p.Glu694=
XM_024452821.1:c.1966_1967delinsGA (MSH6)	XP_024308589.1:p.Glu656=
XM_024452822.1:c.1357_1358delinsGA (MSH6)	XP_024308590.1:p.Glu453=
NM_000179.3:c.2263_2264delinsGA (MSH6) MANE Select	NP_000170.1:p.Glu755=
NM_001281492.2:c.1873_1874delinsGA (MSH6)	NP_001268421.1:p.Glu625=
NM_001281493.2:c.1357_1358delinsGA (MSH6)	NP_001268422.1:p.Glu453=
NM_001281494.2:c.1357_1358delinsGA (MSH6)	NP_001268423.1:p.Glu453=