Canonical Allele Identifier: CA2576961306

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783576_47783577insGT , CM000664.2:g.47783576_47783577insGT	GRCh38
NC_000002.11:g.48010715_48010716insGT , CM000664.1:g.48010715_48010716insGT	GRCh37
NC_000002.10:g.47864219_47864220insGT	NCBI36
NG_007111.1:g.5430_5431insGT , LRG_219:g.5430_5431insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.260+83_260+84insGT	ENSP00000514752.2:n.260+83_260+84insGT
ENST00000699999.1:n.344+83_344+84insGT
ENST00000700000.1:c.260+83_260+84insGT	ENSP00000514749.1:n.260+83_260+84insGT
ENST00000700001.1:n.332+83_332+84insGT
ENST00000700002.1:c.260+83_260+84insGT	ENSP00000514750.1:n.260+83_260+84insGT
ENST00000700003.1:c.260+83_260+84insGT	ENSP00000514751.1:n.260+83_260+84insGT
ENST00000234420.11:c.260+83_260+84insGT MANE Select	ENSP00000234420.5:n.260+83_260+84insGT
ENST00000540021.6:c.237+106_237+107insGT	ENSP00000446475.1:n.237+106_237+107insGT
ENST00000652107.1:c.-37-7351_-37-7350insGT	ENSP00000498629.1:n.-37-7351_-37-7350insGT
ENST00000673637.1:c.-38+345_-38+346insGT	ENSP00000501310.1:n.-38+345_-38+346insGT
ENST00000673922.1:n.349+83_349+84insGT
ENST00000234420.9:c.260+83_260+84insGT	ENSP00000234420.4:n.260+83_260+84insGT
ENST00000445503.5:c.260+83_260+84insGT	ENSP00000405294.1:n.260+83_260+84insGT
ENST00000456246.1:c.260+83_260+84insGT	ENSP00000410570.1:n.260+83_260+84insGT
ENST00000493177.1:n.324+83_324+84insGT
ENST00000540021.5:c.237+106_237+107insGT	ENSP00000446475.1:n.237+106_237+107insGT
ENST00000606499.1:c.-37-7351_-37-7350insGT	ENSP00000475605.1:n.-37-7351_-37-7350insGT
ENST00000614496.4:c.-477+83_-477+84insGT	ENSP00000477844.1:n.-477+83_-477+84insGT
ENST00000616033.4:c.257+83_257+84insGT	ENSP00000480261.1:n.257+83_257+84insGT
ENST00000622629.4:c.-2837+83_-2837+84insGT	ENSP00000482078.1:n.-2837+83_-2837+84insGT
NM_000179.2:c.260+83_260+84insGT , LRG_219t1:c.260+83_260+84insGT	NP_000170.1:n.260+83_260+84insGT
NM_001281492.1:c.237+106_237+107insGT	NP_001268421.1:n.237+106_237+107insGT
NM_001281493.1:c.-477+83_-477+84insGT	NP_001268422.1:n.-477+83_-477+84insGT
XM_011532800.1:c.-38+345_-38+346insGT	XP_011531102.1:n.-38+345_-38+346insGT
XM_024452819.1:c.260+83_260+84insGT	XP_024308587.1:n.260+83_260+84insGT
XM_024452822.1:c.-477+83_-477+84insGT	XP_024308590.1:n.-477+83_-477+84insGT
NM_000179.3:c.260+83_260+84insGT MANE Select	NP_000170.1:n.260+83_260+84insGT
NM_001281492.2:c.237+106_237+107insGT	NP_001268421.1:n.237+106_237+107insGT
NM_001281493.2:c.-477+83_-477+84insGT	NP_001268422.1:n.-477+83_-477+84insGT