Canonical Allele Identifier: CA2496037904
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783118_47783123delinsTTCCTC , CM000664.2:g.47783118_47783123delinsTTCCTC GRCh38
NC_000002.11:g.48010257_48010262delinsTTCCTC , CM000664.1:g.48010257_48010262delinsTTCCTC GRCh37
NC_000002.10:g.47863761_47863766delinsTTCCTC NCBI36
NG_007111.1:g.4972_4977delinsTTCCTC , LRG_219:g.4972_4977delinsTTCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7809_-37-7804delinsTTCCTC ENSP00000498629.1:n.-37-7809_-37-7804delinsTTCCTC
ENST00000234420.9:c.-116_-111delinsTTCCTC ENSP00000234420.4:n.-116_-111delinsTTCCTC
ENST00000445503.5:c.-116_-111delinsTTCCTC ENSP00000405294.1:n.-116_-111delinsTTCCTC
ENST00000540021.5:c.-116_-111delinsTTCCTC ENSP00000446475.1:n.-116_-111delinsTTCCTC
ENST00000606499.1:c.-37-7809_-37-7804delinsTTCCTC ENSP00000475605.1:n.-37-7809_-37-7804delinsTTCCTC
ENST00000614496.4:c.-852_-847delinsTTCCTC ENSP00000477844.1:n.-852_-847delinsTTCCTC
ENST00000622629.4:c.-3212_-3207delinsTTCCTC ENSP00000482078.1:n.-3212_-3207delinsTTCCTC
NM_000179.2:c.-116_-111delinsTTCCTC , LRG_219t1:c.-116_-111delinsTTCCTC NP_000170.1:n.-116_-111delinsTTCCTC
NM_001281492.1:c.-116_-111delinsTTCCTC NP_001268421.1:n.-116_-111delinsTTCCTC
NM_001281493.1:c.-852_-847delinsTTCCTC NP_001268422.1:n.-852_-847delinsTTCCTC