Canonical Allele Identifier: CA2695202207

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805727_47805728insGAAG , CM000664.2:g.47805727_47805728insGAAG	GRCh38
NC_000002.11:g.48032866_48032867insGAAG , CM000664.1:g.48032866_48032867insGAAG	GRCh37
NC_000002.10:g.47886370_47886371insGAAG	NCBI36
NG_007111.1:g.27581_27582insGAAG , LRG_219:g.27581_27582insGAAG
NG_008397.1:g.104948_104949insCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3349+20_3349+21insGAAG (MSH6)	ENSP00000406248.2:n.3349+20_3349+21insGAAG
ENST00000420813.6:c.3349+20_3349+21insGAAG (MSH6)	ENSP00000390382.2:n.3349+20_3349+21insGAAG
ENST00000455383.6:c.3349+20_3349+21insGAAG (MSH6)	ENSP00000397484.2:n.3349+20_3349+21insGAAG
ENST00000700004.2:c.3262+20_3262+21insGAAG (MSH6)	ENSP00000514752.2:n.3262+20_3262+21insGAAG
ENST00000699999.1:n.4320+20_4320+21insGAAG (MSH6)
ENST00000700000.1:c.2080+20_2080+21insGAAG (MSH6)	ENSP00000514749.1:n.2080+20_2080+21insGAAG
ENST00000700002.1:c.3652+20_3652+21insGAAG (MSH6)	ENSP00000514750.1:n.3652+20_3652+21insGAAG
ENST00000700003.1:c.1101+20_1101+21insGAAG (MSH6)	ENSP00000514751.1:n.1101+20_1101+21insGAAG
ENST00000700004.1:c.2419+20_2419+21insGAAG (MSH6)	ENSP00000514752.1:n.2419+20_2419+21insGAAG
ENST00000700005.1:n.2497+20_2497+21insGAAG (MSH6)
ENST00000700006.1:n.4328_4329insGAAG (MSH6)
ENST00000700007.1:n.2241+20_2241+21insGAAG (MSH6)
ENST00000700008.1:n.1815+20_1815+21insGAAG (MSH6)
ENST00000700009.1:n.1834_1835insGAAG (MSH6)
ENST00000700010.1:n.1055+20_1055+21insGAAG (MSH6)
ENST00000700011.1:n.2940+20_2940+21insGAAG (MSH6)
ENST00000234420.11:c.3646+20_3646+21insGAAG (MSH6) MANE Select	ENSP00000234420.5:n.3646+20_3646+21insGAAG
ENST00000540021.6:c.3256+20_3256+21insGAAG (MSH6)	ENSP00000446475.1:n.3256+20_3256+21insGAAG
ENST00000652107.1:c.3349+20_3349+21insGAAG (MSH6)	ENSP00000498629.1:n.3349+20_3349+21insGAAG
ENST00000673637.1:c.3349+20_3349+21insGAAG (MSH6)	ENSP00000501310.1:n.3349+20_3349+21insGAAG
ENST00000234420.9:c.3646+20_3646+21insGAAG (MSH6)	ENSP00000234420.4:n.3646+20_3646+21insGAAG
ENST00000405808.5:c.169+2467_169+2468insCTTC (FBXO11)	ENSP00000385127.1:n.169+2467_169+2468insCTTC
ENST00000434234.5:c.*124+2266_*124+2267insCTTC (FBXO11)	ENSP00000402692.1:n.*124+2266_*124+2267insCTTC
ENST00000445503.5:c.*2993+20_*2993+21insGAAG (MSH6)	ENSP00000405294.1:n.*2993+20_*2993+21insGAAG
ENST00000538136.1:c.2740+20_2740+21insGAAG (MSH6)	ENSP00000438580.1:n.2740+20_2740+21insGAAG
ENST00000540021.5:c.3256+20_3256+21insGAAG (MSH6)	ENSP00000446475.1:n.3256+20_3256+21insGAAG
ENST00000614496.4:c.2740+20_2740+21insGAAG (MSH6)	ENSP00000477844.1:n.2740+20_2740+21insGAAG
ENST00000622629.4:c.550+20_550+21insGAAG (MSH6)	ENSP00000482078.1:n.550+20_550+21insGAAG
NM_000179.2:c.3646+20_3646+21insGAAG , LRG_219t1:c.3646+20_3646+21insGAAG (MSH6)	NP_000170.1:n.3646+20_3646+21insGAAG
NM_001281492.1:c.3256+20_3256+21insGAAG (MSH6)	NP_001268421.1:n.3256+20_3256+21insGAAG
NM_001281493.1:c.2740+20_2740+21insGAAG (MSH6)	NP_001268422.1:n.2740+20_2740+21insGAAG
NM_001281494.1:c.2740+20_2740+21insGAAG (MSH6)	NP_001268423.1:n.2740+20_2740+21insGAAG
XM_005264271.1:c.3349+20_3349+21insGAAG (MSH6)	XP_005264328.1:n.3349+20_3349+21insGAAG
XM_011532798.1:c.3463+20_3463+21insGAAG (MSH6)	XP_011531100.1:n.3463+20_3463+21insGAAG
XM_011532799.1:c.3349+20_3349+21insGAAG (MSH6)	XP_011531101.1:n.3349+20_3349+21insGAAG
XM_011532800.1:c.3349+20_3349+21insGAAG (MSH6)	XP_011531102.1:n.3349+20_3349+21insGAAG
XM_024452819.1:c.3646+20_3646+21insGAAG (MSH6)	XP_024308587.1:n.3646+20_3646+21insGAAG
XM_024452820.1:c.3463+20_3463+21insGAAG (MSH6)	XP_024308588.1:n.3463+20_3463+21insGAAG
XM_024452821.1:c.3349+20_3349+21insGAAG (MSH6)	XP_024308589.1:n.3349+20_3349+21insGAAG
XM_024452822.1:c.2740+20_2740+21insGAAG (MSH6)	XP_024308590.1:n.2740+20_2740+21insGAAG
NM_000179.3:c.3646+20_3646+21insGAAG (MSH6) MANE Select	NP_000170.1:n.3646+20_3646+21insGAAG
NM_001281492.2:c.3256+20_3256+21insGAAG (MSH6)	NP_001268421.1:n.3256+20_3256+21insGAAG
NM_001281493.2:c.2740+20_2740+21insGAAG (MSH6)	NP_001268422.1:n.2740+20_2740+21insGAAG
NM_001281494.2:c.2740+20_2740+21insGAAG (MSH6)	NP_001268423.1:n.2740+20_2740+21insGAAG