Canonical Allele Identifier: CA2496053480

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805637_47805638delinsTG , CM000664.2:g.47805637_47805638delinsTG	GRCh38
NC_000002.11:g.48032776_48032777delinsTG , CM000664.1:g.48032776_48032777delinsTG	GRCh37
NC_000002.10:g.47886280_47886281delinsTG	NCBI36
NG_007111.1:g.27491_27492delinsTG , LRG_219:g.27491_27492delinsTG
NG_008397.1:g.105038_105039delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3279_3280delinsTG (MSH6)	ENSP00000406248.2:p.Val1093=
ENST00000420813.6:c.3279_3280delinsTG (MSH6)	ENSP00000390382.2:p.Val1093=
ENST00000455383.6:c.3279_3280delinsTG (MSH6)	ENSP00000397484.2:p.Val1093=
ENST00000700004.2:c.3192_3193delinsTG (MSH6)	ENSP00000514752.2:p.Val1064=
ENST00000699999.1:n.4250_4251delinsTG (MSH6)
ENST00000700000.1:c.2010_2011delinsTG (MSH6)	ENSP00000514749.1:p.Val670=
ENST00000700002.1:c.3582_3583delinsTG (MSH6)	ENSP00000514750.1:p.Val1194=
ENST00000700003.1:c.1031_1032delinsTG (MSH6)	ENSP00000514751.1:n.1031_1032delinsTG
ENST00000700004.1:c.2349_2350delinsTG (MSH6)	ENSP00000514752.1:p.Val783=
ENST00000700005.1:n.2427_2428delinsTG (MSH6)
ENST00000700006.1:n.4238_4239delinsTG (MSH6)
ENST00000700007.1:n.2171_2172delinsTG (MSH6)
ENST00000700008.1:n.1745_1746delinsTG (MSH6)
ENST00000700009.1:n.1744_1745delinsTG (MSH6)
ENST00000700010.1:n.985_986delinsTG (MSH6)
ENST00000700011.1:n.2870_2871delinsTG (MSH6)
ENST00000234420.11:c.3576_3577delinsTG (MSH6) MANE Select	ENSP00000234420.5:p.Val1192=
ENST00000540021.6:c.3186_3187delinsTG (MSH6)	ENSP00000446475.1:p.Val1062=
ENST00000652107.1:c.3279_3280delinsTG (MSH6)	ENSP00000498629.1:p.Val1093=
ENST00000673637.1:c.3279_3280delinsTG (MSH6)	ENSP00000501310.1:p.Val1093=
ENST00000234420.9:c.3576_3577delinsTG (MSH6)	ENSP00000234420.4:p.Val1192=
ENST00000405808.5:c.169+2557_169+2558delinsCA (FBXO11)	ENSP00000385127.1:n.169+2557_169+2558deli...
ENST00000434234.5:c.*124+2356_*124+2357delinsCA (FBXO11)	ENSP00000402692.1:n.*124+2356_*124+2357de...
ENST00000445503.5:c.*2923_*2924delinsTG (MSH6)	ENSP00000405294.1:n.*2923_*2924delinsTG
ENST00000538136.1:c.2670_2671delinsTG (MSH6)	ENSP00000438580.1:p.Val890=
ENST00000540021.5:c.3186_3187delinsTG (MSH6)	ENSP00000446475.1:p.Val1062=
ENST00000614496.4:c.2670_2671delinsTG (MSH6)	ENSP00000477844.1:p.Val890=
ENST00000622629.4:c.480_481delinsTG (MSH6)	ENSP00000482078.1:p.Val160=
NM_000179.2:c.3576_3577delinsTG , LRG_219t1:c.3576_3577delinsTG (MSH6)	NP_000170.1:p.Val1192=
NM_001281492.1:c.3186_3187delinsTG (MSH6)	NP_001268421.1:p.Val1062=
NM_001281493.1:c.2670_2671delinsTG (MSH6)	NP_001268422.1:p.Val890=
NM_001281494.1:c.2670_2671delinsTG (MSH6)	NP_001268423.1:p.Val890=
XM_005264271.1:c.3279_3280delinsTG (MSH6)	XP_005264328.1:p.Val1093=
XM_011532798.1:c.3393_3394delinsTG (MSH6)	XP_011531100.1:p.Val1131=
XM_011532799.1:c.3279_3280delinsTG (MSH6)	XP_011531101.1:p.Val1093=
XM_011532800.1:c.3279_3280delinsTG (MSH6)	XP_011531102.1:p.Val1093=
XM_024452819.1:c.3576_3577delinsTG (MSH6)	XP_024308587.1:p.Val1192=
XM_024452820.1:c.3393_3394delinsTG (MSH6)	XP_024308588.1:p.Val1131=
XM_024452821.1:c.3279_3280delinsTG (MSH6)	XP_024308589.1:p.Val1093=
XM_024452822.1:c.2670_2671delinsTG (MSH6)	XP_024308590.1:p.Val890=
NM_000179.3:c.3576_3577delinsTG (MSH6) MANE Select	NP_000170.1:p.Val1192=
NM_001281492.2:c.3186_3187delinsTG (MSH6)	NP_001268421.1:p.Val1062=
NM_001281493.2:c.2670_2671delinsTG (MSH6)	NP_001268422.1:p.Val890=
NM_001281494.2:c.2670_2671delinsTG (MSH6)	NP_001268423.1:p.Val890=