Canonical Allele Identifier: CA2496049173

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799978_47799980delinsGTC , CM000664.2:g.47799978_47799980delinsGTC	GRCh38
NC_000002.11:g.48027117_48027119delinsGTC , CM000664.1:g.48027117_48027119delinsGTC	GRCh37
NC_000002.10:g.47880621_47880623delinsGTC	NCBI36
NG_007111.1:g.21832_21834delinsGTC , LRG_219:g.21832_21834delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1698_1700delinsGTC (MSH6)	ENSP00000406248.2:p.Glu566=
ENST00000420813.6:c.1698_1700delinsGTC (MSH6)	ENSP00000390382.2:p.Glu566=
ENST00000455383.6:c.1698_1700delinsGTC (MSH6)	ENSP00000397484.2:p.Glu566=
ENST00000700004.2:c.1995_1997delinsGTC (MSH6)	ENSP00000514752.2:p.Glu665=
ENST00000699999.1:n.2079_2081delinsGTC (MSH6)
ENST00000700000.1:c.1606+389_1606+391delinsGTC (MSH6)	ENSP00000514749.1:n.1606+389_1606+391delinsGTC
ENST00000700002.1:c.2001_2003delinsGTC (MSH6)	ENSP00000514750.1:p.Glu667=
ENST00000700003.1:c.628-3442_628-3440delinsGTC (MSH6)	ENSP00000514751.1:n.628-3442_628-3440delinsGTC
ENST00000700004.1:c.1152_1154delinsGTC (MSH6)	ENSP00000514752.1:p.Glu384=
ENST00000234420.11:c.1995_1997delinsGTC (MSH6) MANE Select	ENSP00000234420.5:p.Glu665=
ENST00000540021.6:c.1605_1607delinsGTC (MSH6)	ENSP00000446475.1:p.Glu535=
ENST00000652107.1:c.1698_1700delinsGTC (MSH6)	ENSP00000498629.1:p.Glu566=
ENST00000673637.1:c.1698_1700delinsGTC (MSH6)	ENSP00000501310.1:p.Glu566=
ENST00000234420.9:c.1995_1997delinsGTC (MSH6)	ENSP00000234420.4:p.Glu665=
ENST00000405808.5:c.169+8215_169+8217delinsGAC (FBXO11)	ENSP00000385127.1:n.169+8215_169+8217delinsGAC
ENST00000434234.5:c.*124+8014_*124+8016delinsGAC (FBXO11)	ENSP00000402692.1:n.*124+8014_*124+8016delinsGAC
ENST00000445503.5:c.*1342_*1344delinsGTC (MSH6)	ENSP00000405294.1:n.*1342_*1344delinsGTC
ENST00000538136.1:c.1089_1091delinsGTC (MSH6)	ENSP00000438580.1:p.Glu363=
ENST00000540021.5:c.1605_1607delinsGTC (MSH6)	ENSP00000446475.1:p.Glu535=
ENST00000614496.4:c.1089_1091delinsGTC (MSH6)	ENSP00000477844.1:p.Glu363=
ENST00000616033.4:c.1992_1994delinsGTC (MSH6)	ENSP00000480261.1:p.Glu664=
ENST00000622629.4:c.-1102_-1100delinsGTC (MSH6)	ENSP00000482078.1:n.-1102_-1100delinsGTC
NM_000179.2:c.1995_1997delinsGTC , LRG_219t1:c.1995_1997delinsGTC (MSH6)	NP_000170.1:p.Glu665=
NM_001281492.1:c.1605_1607delinsGTC (MSH6)	NP_001268421.1:p.Glu535=
NM_001281493.1:c.1089_1091delinsGTC (MSH6)	NP_001268422.1:p.Glu363=
NM_001281494.1:c.1089_1091delinsGTC (MSH6)	NP_001268423.1:p.Glu363=
XM_005264271.1:c.1698_1700delinsGTC (MSH6)	XP_005264328.1:p.Glu566=
XM_011532798.1:c.1812_1814delinsGTC (MSH6)	XP_011531100.1:p.Glu604=
XM_011532799.1:c.1698_1700delinsGTC (MSH6)	XP_011531101.1:p.Glu566=
XM_011532800.1:c.1698_1700delinsGTC (MSH6)	XP_011531102.1:p.Glu566=
XM_024452819.1:c.1995_1997delinsGTC (MSH6)	XP_024308587.1:p.Glu665=
XM_024452820.1:c.1812_1814delinsGTC (MSH6)	XP_024308588.1:p.Glu604=
XM_024452821.1:c.1698_1700delinsGTC (MSH6)	XP_024308589.1:p.Glu566=
XM_024452822.1:c.1089_1091delinsGTC (MSH6)	XP_024308590.1:p.Glu363=
NM_000179.3:c.1995_1997delinsGTC (MSH6) MANE Select	NP_000170.1:p.Glu665=
NM_001281492.2:c.1605_1607delinsGTC (MSH6)	NP_001268421.1:p.Glu535=
NM_001281493.2:c.1089_1091delinsGTC (MSH6)	NP_001268422.1:p.Glu363=
NM_001281494.2:c.1089_1091delinsGTC (MSH6)	NP_001268423.1:p.Glu363=