Canonical Allele Identifier: CA2496037930
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783141C= , CM000664.2:g.47783141C= GRCh38
NC_000002.11:g.48010280C= , CM000664.1:g.48010280C= GRCh37
NC_000002.10:g.47863784C= NCBI36
NG_007111.1:g.4995C= , LRG_219:g.4995C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7786C= ENSP00000498629.1:n.-37-7786C=
ENST00000234420.9:c.-93C= ENSP00000234420.4:n.-93C=
ENST00000445503.5:c.-93C= ENSP00000405294.1:n.-93C=
ENST00000456246.1:c.-93C= ENSP00000410570.1:n.-93C=
ENST00000540021.5:c.-93C= ENSP00000446475.1:n.-93C=
ENST00000606499.1:c.-37-7786C= ENSP00000475605.1:n.-37-7786C=
ENST00000614496.4:c.-829C= ENSP00000477844.1:n.-829C=
ENST00000622629.4:c.-3189C= ENSP00000482078.1:n.-3189C=
NM_000179.2:c.-93C= , LRG_219t1:c.-93C= NP_000170.1:n.-93C=
NM_001281492.1:c.-93C= NP_001268421.1:n.-93C=
NM_001281493.1:c.-829C= NP_001268422.1:n.-829C=