Canonical Allele Identifier: CA2749811828

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783143_47783144dup , CM000664.2:g.47783143_47783144dup	GRCh38
NC_000002.11:g.48010282_48010283dup , CM000664.1:g.48010282_48010283dup	GRCh37
NC_000002.10:g.47863786_47863787dup	NCBI36
NG_007111.1:g.4997_4998dup , LRG_219:g.4997_4998dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7784_-37-7783dup	ENSP00000498629.1:n.-37-7784_-37-7783dup
ENST00000234420.9:c.-91_-90dup	ENSP00000234420.4:n.-91_-90dup
ENST00000445503.5:c.-91_-90dup	ENSP00000405294.1:n.-91_-90dup
ENST00000456246.1:c.-91_-90dup	ENSP00000410570.1:n.-91_-90dup
ENST00000540021.5:c.-91_-90dup	ENSP00000446475.1:n.-91_-90dup
ENST00000606499.1:c.-37-7784_-37-7783dup	ENSP00000475605.1:n.-37-7784_-37-7783dup
ENST00000614496.4:c.-827_-826dup	ENSP00000477844.1:n.-827_-826dup
ENST00000622629.4:c.-3187_-3186dup	ENSP00000482078.1:n.-3187_-3186dup
NM_000179.2:c.-91_-90dup , LRG_219t1:c.-91_-90dup	NP_000170.1:n.-91_-90dup
NM_001281492.1:c.-91_-90dup	NP_001268421.1:n.-91_-90dup
NM_001281493.1:c.-827_-826dup	NP_001268422.1:n.-827_-826dup