Canonical Allele Identifier: CA2586969277

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799175del , CM000664.2:g.47799175del	GRCh38
NC_000002.11:g.48026314del , CM000664.1:g.48026314del	GRCh37
NC_000002.10:g.47879818del	NCBI36
NG_007111.1:g.21029del , LRG_219:g.21029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.895del (MSH6)	ENSP00000406248.2:p.Val299CysfsTer13
ENST00000420813.6:c.895del (MSH6)	ENSP00000390382.2:p.Val299CysfsTer13
ENST00000455383.6:c.895del (MSH6)	ENSP00000397484.2:p.Val299CysfsTer13
ENST00000700004.2:c.1192del (MSH6)	ENSP00000514752.2:p.Val398CysfsTer13
ENST00000699999.1:n.1276del (MSH6)
ENST00000700000.1:c.1192del (MSH6)	ENSP00000514749.1:p.Val398CysfsTer13
ENST00000700002.1:c.1198del (MSH6)	ENSP00000514750.1:p.Val400CysfsTer13
ENST00000700003.1:c.627+3112del (MSH6)	ENSP00000514751.1:n.627+3112del
ENST00000700004.1:c.349del (MSH6)	ENSP00000514752.1:p.Val117CysfsTer13
ENST00000234420.11:c.1192del (MSH6) MANE Select	ENSP00000234420.5:p.Val398CysfsTer13
ENST00000540021.6:c.802del (MSH6)	ENSP00000446475.1:p.Val268CysfsTer13
ENST00000652107.1:c.895del (MSH6)	ENSP00000498629.1:p.Val299CysfsTer13
ENST00000673637.1:c.895del (MSH6)	ENSP00000501310.1:p.Val299CysfsTer13
ENST00000234420.9:c.1192del (MSH6)	ENSP00000234420.4:p.Val398CysfsTer13
ENST00000405808.5:c.169+9020del (FBXO11)	ENSP00000385127.1:n.169+9020del
ENST00000434234.5:c.*124+8819del (FBXO11)	ENSP00000402692.1:n.*124+8819del
ENST00000445503.5:c.*539del (MSH6)	ENSP00000405294.1:n.*539del
ENST00000538136.1:c.286del (MSH6)	ENSP00000438580.1:p.Val96CysfsTer13
ENST00000540021.5:c.802del (MSH6)	ENSP00000446475.1:p.Val268CysfsTer13
ENST00000614496.4:c.286del (MSH6)	ENSP00000477844.1:p.Val96CysfsTer13
ENST00000616033.4:c.1189del (MSH6)	ENSP00000480261.1:p.Val397CysfsTer13
ENST00000622629.4:c.-1905del (MSH6)	ENSP00000482078.1:n.-1905del
NM_000179.2:c.1192del , LRG_219t1:c.1192del (MSH6)	NP_000170.1:p.Val398CysfsTer13
NM_001281492.1:c.802del (MSH6)	NP_001268421.1:p.Val268CysfsTer13
NM_001281493.1:c.286del (MSH6)	NP_001268422.1:p.Val96CysfsTer13
NM_001281494.1:c.286del (MSH6)	NP_001268423.1:p.Val96CysfsTer13
XM_005264271.1:c.895del (MSH6)	XP_005264328.1:p.Val299CysfsTer13
XM_011532798.1:c.1009del (MSH6)	XP_011531100.1:p.Val337CysfsTer13
XM_011532799.1:c.895del (MSH6)	XP_011531101.1:p.Val299CysfsTer13
XM_011532800.1:c.895del (MSH6)	XP_011531102.1:p.Val299CysfsTer13
XM_024452819.1:c.1192del (MSH6)	XP_024308587.1:p.Val398CysfsTer13
XM_024452820.1:c.1009del (MSH6)	XP_024308588.1:p.Val337CysfsTer13
XM_024452821.1:c.895del (MSH6)	XP_024308589.1:p.Val299CysfsTer13
XM_024452822.1:c.286del (MSH6)	XP_024308590.1:p.Val96CysfsTer13
NM_000179.3:c.1192del (MSH6) MANE Select	NP_000170.1:p.Val398CysfsTer13
NM_001281492.2:c.802del (MSH6)	NP_001268421.1:p.Val268CysfsTer13
NM_001281493.2:c.286del (MSH6)	NP_001268422.1:p.Val96CysfsTer13
NM_001281494.2:c.286del (MSH6)	NP_001268423.1:p.Val96CysfsTer13