Canonical Allele Identifier: CA1030294344
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668099757

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783125_47783140del , CM000664.2:g.47783125_47783140del GRCh38
NC_000002.11:g.48010264_48010279del , CM000664.1:g.48010264_48010279del GRCh37
NC_000002.10:g.47863768_47863783del NCBI36
NG_007111.1:g.4979_4994del , LRG_219:g.4979_4994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7802_-37-7787del ENSP00000498629.1:n.-37-7802_-37-7787del
ENST00000234420.9:c.-109_-94del ENSP00000234420.4:n.-109_-94del
ENST00000445503.5:c.-109_-94del ENSP00000405294.1:n.-109_-94del
ENST00000540021.5:c.-109_-94del ENSP00000446475.1:n.-109_-94del
ENST00000606499.1:c.-37-7802_-37-7787del ENSP00000475605.1:n.-37-7802_-37-7787del
ENST00000614496.4:c.-845_-830del ENSP00000477844.1:n.-845_-830del
ENST00000622629.4:c.-3205_-3190del ENSP00000482078.1:n.-3205_-3190del
NM_000179.2:c.-109_-94del , LRG_219t1:c.-109_-94del NP_000170.1:n.-109_-94del
NM_001281492.1:c.-109_-94del NP_001268421.1:n.-109_-94del
NM_001281493.1:c.-845_-830del NP_001268422.1:n.-845_-830del