Canonical Allele Identifier: CA2496037897
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783113C= , CM000664.2:g.47783113C= GRCh38
NC_000002.11:g.48010252C= , CM000664.1:g.48010252C= GRCh37
NC_000002.10:g.47863756C= NCBI36
NG_007111.1:g.4967C= , LRG_219:g.4967C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7814C= ENSP00000498629.1:n.-37-7814C=
ENST00000234420.9:c.-121C= ENSP00000234420.4:n.-121C=
ENST00000445503.5:c.-121C= ENSP00000405294.1:n.-121C=
ENST00000540021.5:c.-121C= ENSP00000446475.1:n.-121C=
ENST00000606499.1:c.-37-7814C= ENSP00000475605.1:n.-37-7814C=
ENST00000614496.4:c.-857C= ENSP00000477844.1:n.-857C=
ENST00000622629.4:c.-3217C= ENSP00000482078.1:n.-3217C=
NM_000179.2:c.-121C= , LRG_219t1:c.-121C= NP_000170.1:n.-121C=
NM_001281492.1:c.-121C= NP_001268421.1:n.-121C=
NM_001281493.1:c.-857C= NP_001268422.1:n.-857C=