Canonical Allele Identifier: CA2496037879

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783097G= , CM000664.2:g.47783097G=	GRCh38
NC_000002.11:g.48010236G= , CM000664.1:g.48010236G=	GRCh37
NC_000002.10:g.47863740G=	NCBI36
NG_007111.1:g.4951G= , LRG_219:g.4951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7830G=	ENSP00000498629.1:n.-37-7830G=
ENST00000234420.9:c.-137G=	ENSP00000234420.4:n.-137G=
ENST00000445503.5:c.-137G=	ENSP00000405294.1:n.-137G=
ENST00000540021.5:c.-137G=	ENSP00000446475.1:n.-137G=
ENST00000606499.1:c.-37-7830G=	ENSP00000475605.1:n.-37-7830G=
ENST00000614496.4:c.-873G=	ENSP00000477844.1:n.-873G=
ENST00000622629.4:c.-3233G=	ENSP00000482078.1:n.-3233G=
NM_000179.2:c.-137G= , LRG_219t1:c.-137G=	NP_000170.1:n.-137G=
NM_001281492.1:c.-137G=	NP_001268421.1:n.-137G=
NM_001281493.1:c.-873G=	NP_001268422.1:n.-873G=