Canonical Allele Identifier: CA46719352

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806257_47806259delinsAAG , CM000664.2:g.47806257_47806259delinsAAG	GRCh38
NC_000002.11:g.48033396_48033398delinsAAG , CM000664.1:g.48033396_48033398delinsAAG	GRCh37
NC_000002.10:g.47886900_47886902delinsAAG	NCBI36
NG_007111.1:g.28111_28113delinsAAG , LRG_219:g.28111_28113delinsAAG
NG_008397.1:g.104417_104419delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3403_3405delinsAAG (MSH6)	ENSP00000406248.2:p.Glu1135Lys
ENST00000420813.6:c.3403_3405delinsAAG (MSH6)	ENSP00000390382.2:p.Glu1135Lys
ENST00000455383.6:c.3403_3405delinsAAG (MSH6)	ENSP00000397484.2:p.Glu1135Lys
ENST00000700004.2:c.3316_3318delinsAAG (MSH6)	ENSP00000514752.2:p.Glu1106Lys
ENST00000699999.1:n.4374_4376delinsAAG (MSH6)
ENST00000700000.1:c.2134_2136delinsAAG (MSH6)	ENSP00000514749.1:p.Glu712Lys
ENST00000700002.1:c.3706_3708delinsAAG (MSH6)	ENSP00000514750.1:p.Glu1236Lys
ENST00000700003.1:c.1155_1157delinsAAG (MSH6)	ENSP00000514751.1:n.1155_1157delinsAAG
ENST00000700004.1:c.2473_2475delinsAAG (MSH6)	ENSP00000514752.1:p.Glu825Lys
ENST00000700005.1:n.2551_2553delinsAAG (MSH6)
ENST00000700006.1:n.4858_4860delinsAAG (MSH6)
ENST00000700007.1:n.2295_2297delinsAAG (MSH6)
ENST00000700008.1:n.1869_1871delinsAAG (MSH6)
ENST00000700009.1:n.2364_2366delinsAAG (MSH6)
ENST00000700010.1:n.1109_1111delinsAAG (MSH6)
ENST00000700011.1:n.2994_2996delinsAAG (MSH6)
ENST00000682451.1:n.4489_4491delinsCTT (FBXO11)
ENST00000684712.1:n.4751_4753delinsCTT (FBXO11)
ENST00000234420.11:c.3700_3702delinsAAG (MSH6) MANE Select	ENSP00000234420.5:p.Glu1234Lys
ENST00000540021.6:c.3310_3312delinsAAG (MSH6)	ENSP00000446475.1:p.Glu1104Lys
ENST00000652107.1:c.3403_3405delinsAAG (MSH6)	ENSP00000498629.1:p.Glu1135Lys
ENST00000673637.1:c.3403_3405delinsAAG (MSH6)	ENSP00000501310.1:p.Glu1135Lys
ENST00000234420.9:c.3700_3702delinsAAG (MSH6)	ENSP00000234420.4:p.Glu1234Lys
ENST00000405808.5:c.169+1936_169+1938delinsCTT (FBXO11)	ENSP00000385127.1:n.169+1936_169+1938delinsCTT
ENST00000434234.5:c.*124+1735_*124+1737delinsCTT (FBXO11)	ENSP00000402692.1:n.*124+1735_*124+1737delinsCTT
ENST00000445503.5:c.*3047_*3049delinsAAG (MSH6)	ENSP00000405294.1:n.*3047_*3049delinsAAG
ENST00000538136.1:c.2794_2796delinsAAG (MSH6)	ENSP00000438580.1:p.Glu932Lys
ENST00000540021.5:c.3310_3312delinsAAG (MSH6)	ENSP00000446475.1:p.Glu1104Lys
ENST00000614496.4:c.2794_2796delinsAAG (MSH6)	ENSP00000477844.1:p.Glu932Lys
ENST00000622629.4:c.604_606delinsAAG (MSH6)	ENSP00000482078.1:p.Glu202Lys
NM_000179.2:c.3700_3702delinsAAG , LRG_219t1:c.3700_3702delinsAAG (MSH6)	NP_000170.1:p.Glu1234Lys
NM_001281492.1:c.3310_3312delinsAAG (MSH6)	NP_001268421.1:p.Glu1104Lys
NM_001281493.1:c.2794_2796delinsAAG (MSH6)	NP_001268422.1:p.Glu932Lys
NM_001281494.1:c.2794_2796delinsAAG (MSH6)	NP_001268423.1:p.Glu932Lys
XM_005264271.1:c.3403_3405delinsAAG (MSH6)	XP_005264328.1:p.Glu1135Lys
XM_011532798.1:c.3517_3519delinsAAG (MSH6)	XP_011531100.1:p.Glu1173Lys
XM_011532799.1:c.3403_3405delinsAAG (MSH6)	XP_011531101.1:p.Glu1135Lys
XM_011532800.1:c.3403_3405delinsAAG (MSH6)	XP_011531102.1:p.Glu1135Lys
XM_024452819.1:c.3700_3702delinsAAG (MSH6)	XP_024308587.1:p.Glu1234Lys
XM_024452820.1:c.3517_3519delinsAAG (MSH6)	XP_024308588.1:p.Glu1173Lys
XM_024452821.1:c.3403_3405delinsAAG (MSH6)	XP_024308589.1:p.Glu1135Lys
XM_024452822.1:c.2794_2796delinsAAG (MSH6)	XP_024308590.1:p.Glu932Lys
NM_000179.3:c.3700_3702delinsAAG (MSH6) MANE Select	NP_000170.1:p.Glu1234Lys
NM_001281492.2:c.3310_3312delinsAAG (MSH6)	NP_001268421.1:p.Glu1104Lys
NM_001281493.2:c.2794_2796delinsAAG (MSH6)	NP_001268422.1:p.Glu932Lys
NM_001281494.2:c.2794_2796delinsAAG (MSH6)	NP_001268423.1:p.Glu932Lys