Canonical Allele Identifier: CA2658965033

Gene: MSH6

Linked Data

• gnomAD v4: 2-47783122-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783124del , CM000664.2:g.47783124del	GRCh38
NC_000002.11:g.48010263del , CM000664.1:g.48010263del	GRCh37
NC_000002.10:g.47863767del	NCBI36
NG_007111.1:g.4978del , LRG_219:g.4978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7803del	ENSP00000498629.1:n.-37-7803del
ENST00000234420.9:c.-110del	ENSP00000234420.4:n.-110del
ENST00000445503.5:c.-110del	ENSP00000405294.1:n.-110del
ENST00000540021.5:c.-110del	ENSP00000446475.1:n.-110del
ENST00000606499.1:c.-37-7803del	ENSP00000475605.1:n.-37-7803del
ENST00000614496.4:c.-846del	ENSP00000477844.1:n.-846del
ENST00000622629.4:c.-3206del	ENSP00000482078.1:n.-3206del
NM_000179.2:c.-110del , LRG_219t1:c.-110del	NP_000170.1:n.-110del
NM_001281492.1:c.-110del	NP_001268421.1:n.-110del
NM_001281493.1:c.-846del	NP_001268422.1:n.-846del