Canonical Allele Identifier: CA2695200601

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2673721
• ClinVar RCV Id: RCV003450358

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806253_47806274dup , CM000664.2:g.47806253_47806274dup	GRCh38
NC_000002.11:g.48033392_48033413dup , CM000664.1:g.48033392_48033413dup	GRCh37
NC_000002.10:g.47886896_47886917dup	NCBI36
NG_007111.1:g.28107_28128dup , LRG_219:g.28107_28128dup
NG_008397.1:g.104402_104423dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3399_3420dup (MSH6)	ENSP00000406248.2:p.Lys1141Ter
ENST00000420813.6:c.3399_3420dup (MSH6)	ENSP00000390382.2:p.Lys1141Ter
ENST00000455383.6:c.3399_3420dup (MSH6)	ENSP00000397484.2:p.Lys1141Ter
ENST00000700004.2:c.3312_3333dup (MSH6)	ENSP00000514752.2:p.Lys1112Ter
ENST00000699999.1:n.4370_4391dup (MSH6)
ENST00000700000.1:c.2130_2151dup (MSH6)	ENSP00000514749.1:p.Lys718Ter
ENST00000700002.1:c.3702_3723dup (MSH6)	ENSP00000514750.1:p.Lys1242Ter
ENST00000700003.1:c.1151_1172dup (MSH6)	ENSP00000514751.1:n.1151_1172dup
ENST00000700004.1:c.2469_2490dup (MSH6)	ENSP00000514752.1:p.Lys831Ter
ENST00000700005.1:n.2547_2568dup (MSH6)
ENST00000700006.1:n.4854_4875dup (MSH6)
ENST00000700007.1:n.2291_2312dup (MSH6)
ENST00000700008.1:n.1865_1886dup (MSH6)
ENST00000700009.1:n.2360_2381dup (MSH6)
ENST00000700010.1:n.1105_1126dup (MSH6)
ENST00000700011.1:n.2990_3011dup (MSH6)
ENST00000682451.1:n.4474_4495dup (FBXO11)
ENST00000684712.1:n.4736_4757dup (FBXO11)
ENST00000234420.11:c.3696_3717dup (MSH6) MANE Select	ENSP00000234420.5:p.Lys1240Ter
ENST00000540021.6:c.3306_3327dup (MSH6)	ENSP00000446475.1:p.Lys1110Ter
ENST00000652107.1:c.3399_3420dup (MSH6)	ENSP00000498629.1:p.Lys1141Ter
ENST00000673637.1:c.3399_3420dup (MSH6)	ENSP00000501310.1:p.Lys1141Ter
ENST00000234420.9:c.3696_3717dup (MSH6)	ENSP00000234420.4:p.Lys1240Ter
ENST00000405808.5:c.169+1921_169+1942dup (FBXO11)	ENSP00000385127.1:n.169+1921_169+1942dup
ENST00000434234.5:c.*124+1720_*124+1741dup (FBXO11)	ENSP00000402692.1:n.*124+1720_*124+1741dup
ENST00000445503.5:c.*3043_*3064dup (MSH6)	ENSP00000405294.1:n.*3043_*3064dup
ENST00000538136.1:c.2790_2811dup (MSH6)	ENSP00000438580.1:p.Lys938Ter
ENST00000540021.5:c.3306_3327dup (MSH6)	ENSP00000446475.1:p.Lys1110Ter
ENST00000614496.4:c.2790_2811dup (MSH6)	ENSP00000477844.1:p.Lys938Ter
ENST00000622629.4:c.600_621dup (MSH6)	ENSP00000482078.1:p.Lys208Ter
NM_000179.2:c.3696_3717dup , LRG_219t1:c.3696_3717dup (MSH6)	NP_000170.1:p.Lys1240Ter
NM_001281492.1:c.3306_3327dup (MSH6)	NP_001268421.1:p.Lys1110Ter
NM_001281493.1:c.2790_2811dup (MSH6)	NP_001268422.1:p.Lys938Ter
NM_001281494.1:c.2790_2811dup (MSH6)	NP_001268423.1:p.Lys938Ter
XM_005264271.1:c.3399_3420dup (MSH6)	XP_005264328.1:p.Lys1141Ter
XM_011532798.1:c.3513_3534dup (MSH6)	XP_011531100.1:p.Lys1179Ter
XM_011532799.1:c.3399_3420dup (MSH6)	XP_011531101.1:p.Lys1141Ter
XM_011532800.1:c.3399_3420dup (MSH6)	XP_011531102.1:p.Lys1141Ter
XM_024452819.1:c.3696_3717dup (MSH6)	XP_024308587.1:p.Lys1240Ter
XM_024452820.1:c.3513_3534dup (MSH6)	XP_024308588.1:p.Lys1179Ter
XM_024452821.1:c.3399_3420dup (MSH6)	XP_024308589.1:p.Lys1141Ter
XM_024452822.1:c.2790_2811dup (MSH6)	XP_024308590.1:p.Lys938Ter
NM_000179.3:c.3696_3717dup (MSH6) MANE Select	NP_000170.1:p.Lys1240Ter
NM_001281492.2:c.3306_3327dup (MSH6)	NP_001268421.1:p.Lys1110Ter
NM_001281493.2:c.2790_2811dup (MSH6)	NP_001268422.1:p.Lys938Ter
NM_001281494.2:c.2790_2811dup (MSH6)	NP_001268423.1:p.Lys938Ter