Canonical Allele Identifier: CA2496037939

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783148T= , CM000664.2:g.47783148T=	GRCh38
NC_000002.11:g.48010287T= , CM000664.1:g.48010287T=	GRCh37
NC_000002.10:g.47863791T=	NCBI36
NG_007111.1:g.5002T= , LRG_219:g.5002T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234420.11:c.-86T= MANE Select	ENSP00000234420.5:n.-86T=
ENST00000652107.1:c.-37-7779T=	ENSP00000498629.1:n.-37-7779T=
ENST00000673922.1:n.4T=
ENST00000234420.9:c.-86T=	ENSP00000234420.4:n.-86T=
ENST00000445503.5:c.-86T=	ENSP00000405294.1:n.-86T=
ENST00000456246.1:c.-86T=	ENSP00000410570.1:n.-86T=
ENST00000540021.5:c.-86T=	ENSP00000446475.1:n.-86T=
ENST00000606499.1:c.-37-7779T=	ENSP00000475605.1:n.-37-7779T=
ENST00000614496.4:c.-822T=	ENSP00000477844.1:n.-822T=
ENST00000622629.4:c.-3182T=	ENSP00000482078.1:n.-3182T=
NM_000179.2:c.-86T= , LRG_219t1:c.-86T=	NP_000170.1:n.-86T=
NM_001281492.1:c.-86T=	NP_001268421.1:n.-86T=
NM_001281493.1:c.-822T=	NP_001268422.1:n.-822T=
XM_024452819.1:c.-86T=	XP_024308587.1:n.-86T=
NM_000179.3:c.-86T= MANE Select	NP_000170.1:n.-86T=
NM_001281492.2:c.-86T=	NP_001268421.1:n.-86T=
NM_001281493.2:c.-822T=	NP_001268422.1:n.-822T=