Canonical Allele Identifier: CA071753

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806165_47806169del , CM000664.2:g.47806165_47806169del	GRCh38
NC_000002.11:g.48033304_48033308del , CM000664.1:g.48033304_48033308del	GRCh37
NC_000002.10:g.47886808_47886812del	NCBI36
NG_007111.1:g.28019_28023del , LRG_219:g.28019_28023del
NG_008397.1:g.104509_104513del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3350-39_3350-35del (MSH6)	ENSP00000406248.2:n.3350-39_3350-35del
ENST00000420813.6:c.3350-39_3350-35del (MSH6)	ENSP00000390382.2:n.3350-39_3350-35del
ENST00000455383.6:c.3350-39_3350-35del (MSH6)	ENSP00000397484.2:n.3350-39_3350-35del
ENST00000700004.2:c.3263-39_3263-35del (MSH6)	ENSP00000514752.2:n.3263-39_3263-35del
ENST00000699999.1:n.4321-39_4321-35del (MSH6)
ENST00000700000.1:c.2081-39_2081-35del (MSH6)	ENSP00000514749.1:n.2081-39_2081-35del
ENST00000700002.1:c.3653-39_3653-35del (MSH6)	ENSP00000514750.1:n.3653-39_3653-35del
ENST00000700003.1:c.1102-39_1102-35del (MSH6)	ENSP00000514751.1:n.1102-39_1102-35del
ENST00000700004.1:c.2420-39_2420-35del (MSH6)	ENSP00000514752.1:n.2420-39_2420-35del
ENST00000700005.1:n.2498-39_2498-35del (MSH6)
ENST00000700006.1:n.4766_4770del (MSH6)
ENST00000700007.1:n.2242-39_2242-35del (MSH6)
ENST00000700008.1:n.1816-39_1816-35del (MSH6)
ENST00000700009.1:n.2272_2276del (MSH6)
ENST00000700010.1:n.1056-39_1056-35del (MSH6)
ENST00000700011.1:n.2941-39_2941-35del (MSH6)
ENST00000682451.1:n.4581_4585del (FBXO11)
ENST00000684712.1:n.4843_4847del (FBXO11)
ENST00000234420.11:c.3647-39_3647-35del (MSH6) MANE Select	ENSP00000234420.5:n.3647-39_3647-35del
ENST00000540021.6:c.3257-39_3257-35del (MSH6)	ENSP00000446475.1:n.3257-39_3257-35del
ENST00000652107.1:c.3350-39_3350-35del (MSH6)	ENSP00000498629.1:n.3350-39_3350-35del
ENST00000673637.1:c.3350-39_3350-35del (MSH6)	ENSP00000501310.1:n.3350-39_3350-35del
ENST00000234420.9:c.3647-39_3647-35del (MSH6)	ENSP00000234420.4:n.3647-39_3647-35del
ENST00000405808.5:c.169+2028_169+2032del (FBXO11)	ENSP00000385127.1:n.169+2028_169+2032del
ENST00000434234.5:c.*124+1827_*124+1831del (FBXO11)	ENSP00000402692.1:n.*124+1827_*124+1831de...
ENST00000445503.5:c.*2994-39_*2994-35del (MSH6)	ENSP00000405294.1:n.*2994-39_*2994-35del
ENST00000538136.1:c.2741-39_2741-35del (MSH6)	ENSP00000438580.1:n.2741-39_2741-35del
ENST00000540021.5:c.3257-39_3257-35del (MSH6)	ENSP00000446475.1:n.3257-39_3257-35del
ENST00000614496.4:c.2741-39_2741-35del (MSH6)	ENSP00000477844.1:n.2741-39_2741-35del
ENST00000622629.4:c.551-39_551-35del (MSH6)	ENSP00000482078.1:n.551-39_551-35del
NM_000179.2:c.3647-39_3647-35del , LRG_219t1:c.3647-39_3647-35del (MSH6)	NP_000170.1:n.3647-39_3647-35del
NM_001281492.1:c.3257-39_3257-35del (MSH6)	NP_001268421.1:n.3257-39_3257-35del
NM_001281493.1:c.2741-39_2741-35del (MSH6)	NP_001268422.1:n.2741-39_2741-35del
NM_001281494.1:c.2741-39_2741-35del (MSH6)	NP_001268423.1:n.2741-39_2741-35del
XM_005264271.1:c.3350-39_3350-35del (MSH6)	XP_005264328.1:n.3350-39_3350-35del
XM_011532798.1:c.3464-39_3464-35del (MSH6)	XP_011531100.1:n.3464-39_3464-35del
XM_011532799.1:c.3350-39_3350-35del (MSH6)	XP_011531101.1:n.3350-39_3350-35del
XM_011532800.1:c.3350-39_3350-35del (MSH6)	XP_011531102.1:n.3350-39_3350-35del
XM_024452819.1:c.3647-39_3647-35del (MSH6)	XP_024308587.1:n.3647-39_3647-35del
XM_024452820.1:c.3464-39_3464-35del (MSH6)	XP_024308588.1:n.3464-39_3464-35del
XM_024452821.1:c.3350-39_3350-35del (MSH6)	XP_024308589.1:n.3350-39_3350-35del
XM_024452822.1:c.2741-39_2741-35del (MSH6)	XP_024308590.1:n.2741-39_2741-35del
NM_000179.3:c.3647-39_3647-35del (MSH6) MANE Select	NP_000170.1:n.3647-39_3647-35del
NM_001281492.2:c.3257-39_3257-35del (MSH6)	NP_001268421.1:n.3257-39_3257-35del
NM_001281493.2:c.2741-39_2741-35del (MSH6)	NP_001268422.1:n.2741-39_2741-35del
NM_001281494.2:c.2741-39_2741-35del (MSH6)	NP_001268423.1:n.2741-39_2741-35del