Canonical Allele Identifier: CA769515817

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1226098214
• MyVariant Identifiers: chr2:g.48028020_48028025del (hg19) ; chr2:g.47800881_47800886del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800882_47800887del , CM000664.2:g.47800882_47800887del	GRCh38
NC_000002.11:g.48028021_48028026del , CM000664.1:g.48028021_48028026del	GRCh37
NC_000002.10:g.47881525_47881530del	NCBI36
NG_007111.1:g.22736_22741del , LRG_219:g.22736_22741del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2602_2607del (MSH6)	ENSP00000406248.2:p.Ile868_Val869del
ENST00000420813.6:c.2602_2607del (MSH6)	ENSP00000390382.2:p.Ile868_Val869del
ENST00000455383.6:c.2602_2607del (MSH6)	ENSP00000397484.2:p.Ile868_Val869del
ENST00000700004.2:c.2899_2904del (MSH6)	ENSP00000514752.2:p.Ile967_Val968del
ENST00000699999.1:n.2983_2988del (MSH6)
ENST00000700000.1:c.1606+1293_1606+1298del (MSH6)	ENSP00000514749.1:n.1606+1293_1606+1298de...
ENST00000700002.1:c.2905_2910del (MSH6)	ENSP00000514750.1:p.Ile969_Val970del
ENST00000700003.1:c.628-2538_628-2533del (MSH6)	ENSP00000514751.1:n.628-2538_628-2533del
ENST00000700004.1:c.2056_2061del (MSH6)	ENSP00000514752.1:p.Ile686_Val687del
ENST00000234420.11:c.2899_2904del (MSH6) MANE Select	ENSP00000234420.5:p.Ile967_Val968del
ENST00000540021.6:c.2509_2514del (MSH6)	ENSP00000446475.1:p.Ile837_Val838del
ENST00000652107.1:c.2602_2607del (MSH6)	ENSP00000498629.1:p.Ile868_Val869del
ENST00000673637.1:c.2602_2607del (MSH6)	ENSP00000501310.1:p.Ile868_Val869del
ENST00000234420.9:c.2899_2904del (MSH6)	ENSP00000234420.4:p.Ile967_Val968del
ENST00000405808.5:c.169+7309_169+7314del (FBXO11)	ENSP00000385127.1:n.169+7309_169+7314del
ENST00000434234.5:c.*124+7108_*124+7113del (FBXO11)	ENSP00000402692.1:n.*124+7108_*124+7113de...
ENST00000445503.5:c.*2246_*2251del (MSH6)	ENSP00000405294.1:n.*2246_*2251del
ENST00000538136.1:c.1993_1998del (MSH6)	ENSP00000438580.1:p.Ile665_Val666del
ENST00000540021.5:c.2509_2514del (MSH6)	ENSP00000446475.1:p.Ile837_Val838del
ENST00000614496.4:c.1993_1998del (MSH6)	ENSP00000477844.1:p.Ile665_Val666del
ENST00000616033.4:c.2896_2901del (MSH6)	ENSP00000480261.1:p.Ile966_Val967del
ENST00000622629.4:c.-198_-193del (MSH6)	ENSP00000482078.1:n.-198_-193del
NM_000179.2:c.2899_2904del , LRG_219t1:c.2899_2904del (MSH6)	NP_000170.1:p.Ile967_Val968del
NM_001281492.1:c.2509_2514del (MSH6)	NP_001268421.1:p.Ile837_Val838del
NM_001281493.1:c.1993_1998del (MSH6)	NP_001268422.1:p.Ile665_Val666del
NM_001281494.1:c.1993_1998del (MSH6)	NP_001268423.1:p.Ile665_Val666del
XM_005264271.1:c.2602_2607del (MSH6)	XP_005264328.1:p.Ile868_Val869del
XM_011532798.1:c.2716_2721del (MSH6)	XP_011531100.1:p.Ile906_Val907del
XM_011532799.1:c.2602_2607del (MSH6)	XP_011531101.1:p.Ile868_Val869del
XM_011532800.1:c.2602_2607del (MSH6)	XP_011531102.1:p.Ile868_Val869del
XM_024452819.1:c.2899_2904del (MSH6)	XP_024308587.1:p.Ile967_Val968del
XM_024452820.1:c.2716_2721del (MSH6)	XP_024308588.1:p.Ile906_Val907del
XM_024452821.1:c.2602_2607del (MSH6)	XP_024308589.1:p.Ile868_Val869del
XM_024452822.1:c.1993_1998del (MSH6)	XP_024308590.1:p.Ile665_Val666del
NM_000179.3:c.2899_2904del (MSH6) MANE Select	NP_000170.1:p.Ile967_Val968del
NM_001281492.2:c.2509_2514del (MSH6)	NP_001268421.1:p.Ile837_Val838del
NM_001281493.2:c.1993_1998del (MSH6)	NP_001268422.1:p.Ile665_Val666del
NM_001281494.2:c.1993_1998del (MSH6)	NP_001268423.1:p.Ile665_Val666del