Canonical Allele Identifier: CA2580066988

Gene: MSH6

Linked Data

• ClinVar Variation Id: 1766180
• ClinVar RCV Id: RCV002371243

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783325_47783334del , CM000664.2:g.47783325_47783334del	GRCh38
NC_000002.11:g.48010464_48010473del , CM000664.1:g.48010464_48010473del	GRCh37
NC_000002.10:g.47863968_47863977del	NCBI36
NG_007111.1:g.5179_5188del , LRG_219:g.5179_5188del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700004.2:c.92_101del	ENSP00000514752.2:p.Gly31AlafsTer?
ENST00000699999.1:n.176_185del
ENST00000700000.1:c.92_101del	ENSP00000514749.1:p.Gly31AlafsTer?
ENST00000700001.1:n.164_173del
ENST00000700002.1:c.92_101del	ENSP00000514750.1:p.Gly31AlafsTer?
ENST00000700003.1:c.92_101del	ENSP00000514751.1:p.Gly31AlafsTer?
ENST00000234420.11:c.92_101del MANE Select	ENSP00000234420.5:p.Gly31AlafsTer?
ENST00000540021.6:c.92_101del	ENSP00000446475.1:p.Gly31AlafsTer?
ENST00000652107.1:c.-37-7602_-37-7593del	ENSP00000498629.1:n.-37-7602_-37-7593del
ENST00000673637.1:c.-38+94_-38+103del	ENSP00000501310.1:n.-38+94_-38+103del
ENST00000673922.1:n.181_190del
ENST00000234420.9:c.92_101del	ENSP00000234420.4:p.Gly31AlafsTer?
ENST00000445503.5:c.92_101del	ENSP00000405294.1:p.Gly31AlafsTer?
ENST00000456246.1:c.92_101del	ENSP00000410570.1:p.Gly31AlafsTer?
ENST00000493177.1:n.156_165del
ENST00000540021.5:c.92_101del	ENSP00000446475.1:p.Gly31AlafsTer?
ENST00000606499.1:c.-37-7602_-37-7593del	ENSP00000475605.1:n.-37-7602_-37-7593del
ENST00000614496.4:c.-645_-636del	ENSP00000477844.1:n.-645_-636del
ENST00000616033.4:c.92_101del	ENSP00000480261.1:p.Gly31AlafsTer?
ENST00000622629.4:c.-3005_-2996del	ENSP00000482078.1:n.-3005_-2996del
NM_000179.2:c.92_101del , LRG_219t1:c.92_101del	NP_000170.1:p.Gly31AlafsTer?
NM_001281492.1:c.92_101del	NP_001268421.1:p.Gly31AlafsTer?
NM_001281493.1:c.-645_-636del	NP_001268422.1:n.-645_-636del
XM_011532800.1:c.-38+94_-38+103del	XP_011531102.1:n.-38+94_-38+103del
XM_024452819.1:c.92_101del	XP_024308587.1:p.Gly31AlafsTer?
XM_024452822.1:c.-645_-636del	XP_024308590.1:n.-645_-636del
NM_000179.3:c.92_101del MANE Select	NP_000170.1:p.Gly31AlafsTer?
NM_001281492.2:c.92_101del	NP_001268421.1:p.Gly31AlafsTer?
NM_001281493.2:c.-645_-636del	NP_001268422.1:n.-645_-636del