Canonical Allele Identifier: CA2571681055
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782996_47783000dup , CM000664.2:g.47782996_47783000dup GRCh38
NC_000002.11:g.48010135_48010139dup , CM000664.1:g.48010135_48010139dup GRCh37
NC_000002.10:g.47863639_47863643dup NCBI36
NG_007111.1:g.4850_4854dup , LRG_219:g.4850_4854dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7931_-37-7927dup ENSP00000498629.1:n.-37-7931_-37-7927dup
ENST00000606499.1:c.-37-7931_-37-7927dup ENSP00000475605.1:n.-37-7931_-37-7927dup