Canonical Allele Identifier: CA2496049933

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800880_47800886delinsCCATAGT , CM000664.2:g.47800880_47800886delinsCCATAGT	GRCh38
NC_000002.11:g.48028019_48028025delinsCCATAGT , CM000664.1:g.48028019_48028025delinsCCATAGT	GRCh37
NC_000002.10:g.47881523_47881529delinsCCATAGT	NCBI36
NG_007111.1:g.22734_22740delinsCCATAGT , LRG_219:g.22734_22740delinsCCATAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2600_2606delinsCCATAGT (MSH6)	ENSP00000406248.2:p.Thr867=
ENST00000420813.6:c.2600_2606delinsCCATAGT (MSH6)	ENSP00000390382.2:p.Thr867=
ENST00000455383.6:c.2600_2606delinsCCATAGT (MSH6)	ENSP00000397484.2:p.Thr867=
ENST00000700004.2:c.2897_2903delinsCCATAGT (MSH6)	ENSP00000514752.2:p.Thr966=
ENST00000699999.1:n.2981_2987delinsCCATAGT (MSH6)
ENST00000700000.1:c.1606+1291_1606+1297delinsCCATAGT (MSH6)	ENSP00000514749.1:n.1606+1291_1606+1297de...
ENST00000700002.1:c.2903_2909delinsCCATAGT (MSH6)	ENSP00000514750.1:p.Thr968=
ENST00000700003.1:c.628-2540_628-2534delinsCCATAGT (MSH6)	ENSP00000514751.1:n.628-2540_628-2534deli...
ENST00000700004.1:c.2054_2060delinsCCATAGT (MSH6)	ENSP00000514752.1:p.Thr685=
ENST00000234420.11:c.2897_2903delinsCCATAGT (MSH6) MANE Select	ENSP00000234420.5:p.Thr966=
ENST00000540021.6:c.2507_2513delinsCCATAGT (MSH6)	ENSP00000446475.1:p.Thr836=
ENST00000652107.1:c.2600_2606delinsCCATAGT (MSH6)	ENSP00000498629.1:p.Thr867=
ENST00000673637.1:c.2600_2606delinsCCATAGT (MSH6)	ENSP00000501310.1:p.Thr867=
ENST00000234420.9:c.2897_2903delinsCCATAGT (MSH6)	ENSP00000234420.4:p.Thr966=
ENST00000405808.5:c.169+7309_169+7315delinsACTATGG (FBXO11)	ENSP00000385127.1:n.169+7309_169+7315deli...
ENST00000434234.5:c.*124+7108_*124+7114delinsACTATGG (FBXO11)	ENSP00000402692.1:n.*124+7108_*124+7114de...
ENST00000445503.5:c.*2244_*2250delinsCCATAGT (MSH6)	ENSP00000405294.1:n.*2244_*2250delinsCCAT...
ENST00000538136.1:c.1991_1997delinsCCATAGT (MSH6)	ENSP00000438580.1:p.Thr664=
ENST00000540021.5:c.2507_2513delinsCCATAGT (MSH6)	ENSP00000446475.1:p.Thr836=
ENST00000614496.4:c.1991_1997delinsCCATAGT (MSH6)	ENSP00000477844.1:p.Thr664=
ENST00000616033.4:c.2894_2900delinsCCATAGT (MSH6)	ENSP00000480261.1:p.Thr965=
ENST00000622629.4:c.-200_-194delinsCCATAGT (MSH6)	ENSP00000482078.1:n.-200_-194delinsCCATAG...
NM_000179.2:c.2897_2903delinsCCATAGT , LRG_219t1:c.2897_2903delinsCCATAGT (MSH6)	NP_000170.1:p.Thr966=
NM_001281492.1:c.2507_2513delinsCCATAGT (MSH6)	NP_001268421.1:p.Thr836=
NM_001281493.1:c.1991_1997delinsCCATAGT (MSH6)	NP_001268422.1:p.Thr664=
NM_001281494.1:c.1991_1997delinsCCATAGT (MSH6)	NP_001268423.1:p.Thr664=
XM_005264271.1:c.2600_2606delinsCCATAGT (MSH6)	XP_005264328.1:p.Thr867=
XM_011532798.1:c.2714_2720delinsCCATAGT (MSH6)	XP_011531100.1:p.Thr905=
XM_011532799.1:c.2600_2606delinsCCATAGT (MSH6)	XP_011531101.1:p.Thr867=
XM_011532800.1:c.2600_2606delinsCCATAGT (MSH6)	XP_011531102.1:p.Thr867=
XM_024452819.1:c.2897_2903delinsCCATAGT (MSH6)	XP_024308587.1:p.Thr966=
XM_024452820.1:c.2714_2720delinsCCATAGT (MSH6)	XP_024308588.1:p.Thr905=
XM_024452821.1:c.2600_2606delinsCCATAGT (MSH6)	XP_024308589.1:p.Thr867=
XM_024452822.1:c.1991_1997delinsCCATAGT (MSH6)	XP_024308590.1:p.Thr664=
NM_000179.3:c.2897_2903delinsCCATAGT (MSH6) MANE Select	NP_000170.1:p.Thr966=
NM_001281492.2:c.2507_2513delinsCCATAGT (MSH6)	NP_001268421.1:p.Thr836=
NM_001281493.2:c.1991_1997delinsCCATAGT (MSH6)	NP_001268422.1:p.Thr664=
NM_001281494.2:c.1991_1997delinsCCATAGT (MSH6)	NP_001268423.1:p.Thr664=