Canonical Allele Identifier: CA2699269505

Gene: MSH6

Linked Data

• dbSNP Id: rs2103947160

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783548_47783549insGGCAGCACTGTCTG , CM000664.2:g.47783548_47783549insGGCAGCACTGTCTG	GRCh38
NC_000002.11:g.48010687_48010688insGGCAGCACTGTCTG , CM000664.1:g.48010687_48010688insGGCAGCACTGTCTG	GRCh37
NC_000002.10:g.47864191_47864192insGGCAGCACTGTCTG	NCBI36
NG_007111.1:g.5402_5403insGGCAGCACTGTCTG , LRG_219:g.5402_5403insGGCAGCACTGTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000514752.2:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000699999.1:n.344+55_344+56insGGCAGCACTGTCTG
ENST00000700000.1:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000514749.1:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000700001.1:n.332+55_332+56insGGCAGCACTGTCTG
ENST00000700002.1:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000514750.1:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000700003.1:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000514751.1:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000234420.11:c.260+55_260+56insGGCAGCACTGTCTG MANE Select	ENSP00000234420.5:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000540021.6:c.237+78_237+79insGGCAGCACTGTCTG	ENSP00000446475.1:n.237+78_237+79insGGCAGCACTGTCTG
ENST00000652107.1:c.-37-7379_-37-7378insGGCAGCACTGTCTG	ENSP00000498629.1:n.-37-7379_-37-7378insGGCAGCACTGTCTG
ENST00000673637.1:c.-38+317_-38+318insGGCAGCACTGTCTG	ENSP00000501310.1:n.-38+317_-38+318insGGCAGCACTGTCTG
ENST00000673922.1:n.349+55_349+56insGGCAGCACTGTCTG
ENST00000234420.9:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000234420.4:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000445503.5:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000405294.1:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000456246.1:c.260+55_260+56insGGCAGCACTGTCTG	ENSP00000410570.1:n.260+55_260+56insGGCAGCACTGTCTG
ENST00000493177.1:n.324+55_324+56insGGCAGCACTGTCTG
ENST00000540021.5:c.237+78_237+79insGGCAGCACTGTCTG	ENSP00000446475.1:n.237+78_237+79insGGCAGCACTGTCTG
ENST00000606499.1:c.-37-7379_-37-7378insGGCAGCACTGTCTG	ENSP00000475605.1:n.-37-7379_-37-7378insGGCAGCACTGTCTG
ENST00000614496.4:c.-477+55_-477+56insGGCAGCACTGTCTG	ENSP00000477844.1:n.-477+55_-477+56insGGCAGCACTGTCTG
ENST00000616033.4:c.257+55_257+56insGGCAGCACTGTCTG	ENSP00000480261.1:n.257+55_257+56insGGCAGCACTGTCTG
ENST00000622629.4:c.-2837+55_-2837+56insGGCAGCACTGTCTG	ENSP00000482078.1:n.-2837+55_-2837+56insGGCAGCACTGTCTG
NM_000179.2:c.260+55_260+56insGGCAGCACTGTCTG , LRG_219t1:c.260+55_260+56insGGCAGCACTGTCTG	NP_000170.1:n.260+55_260+56insGGCAGCACTGTCTG
NM_001281492.1:c.237+78_237+79insGGCAGCACTGTCTG	NP_001268421.1:n.237+78_237+79insGGCAGCACTGTCTG
NM_001281493.1:c.-477+55_-477+56insGGCAGCACTGTCTG	NP_001268422.1:n.-477+55_-477+56insGGCAGCACTGTCTG
XM_011532800.1:c.-38+317_-38+318insGGCAGCACTGTCTG	XP_011531102.1:n.-38+317_-38+318insGGCAGCACTGTCTG
XM_024452819.1:c.260+55_260+56insGGCAGCACTGTCTG	XP_024308587.1:n.260+55_260+56insGGCAGCACTGTCTG
XM_024452822.1:c.-477+55_-477+56insGGCAGCACTGTCTG	XP_024308590.1:n.-477+55_-477+56insGGCAGCACTGTCTG
NM_000179.3:c.260+55_260+56insGGCAGCACTGTCTG MANE Select	NP_000170.1:n.260+55_260+56insGGCAGCACTGTCTG
NM_001281492.2:c.237+78_237+79insGGCAGCACTGTCTG	NP_001268421.1:n.237+78_237+79insGGCAGCACTGTCTG
NM_001281493.2:c.-477+55_-477+56insGGCAGCACTGTCTG	NP_001268422.1:n.-477+55_-477+56insGGCAGCACTGTCTG