Canonical Allele Identifier: CA2496037982

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783195T= , CM000664.2:g.47783195T=	GRCh38
NC_000002.11:g.48010334T= , CM000664.1:g.48010334T=	GRCh37
NC_000002.10:g.47863838T=	NCBI36
NG_007111.1:g.5049T= , LRG_219:g.5049T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.-39T=	ENSP00000514752.2:n.-39T=
ENST00000699999.1:n.46T=
ENST00000700000.1:c.-39T=	ENSP00000514749.1:n.-39T=
ENST00000700001.1:n.34T=
ENST00000700002.1:c.-39T=	ENSP00000514750.1:n.-39T=
ENST00000234420.11:c.-39T= MANE Select	ENSP00000234420.5:n.-39T=
ENST00000540021.6:c.-39T=	ENSP00000446475.1:n.-39T=
ENST00000652107.1:c.-37-7732T=	ENSP00000498629.1:n.-37-7732T=
ENST00000673637.1:c.-74T=	ENSP00000501310.1:n.-74T=
ENST00000673922.1:n.51T=
ENST00000234420.9:c.-39T=	ENSP00000234420.4:n.-39T=
ENST00000445503.5:c.-39T=	ENSP00000405294.1:n.-39T=
ENST00000456246.1:c.-39T=	ENSP00000410570.1:n.-39T=
ENST00000493177.1:n.26T=
ENST00000540021.5:c.-39T=	ENSP00000446475.1:n.-39T=
ENST00000606499.1:c.-37-7732T=	ENSP00000475605.1:n.-37-7732T=
ENST00000614496.4:c.-775T=	ENSP00000477844.1:n.-775T=
ENST00000616033.4:c.-39T=	ENSP00000480261.1:n.-39T=
ENST00000622629.4:c.-3135T=	ENSP00000482078.1:n.-3135T=
NM_000179.2:c.-39T= , LRG_219t1:c.-39T=	NP_000170.1:n.-39T=
NM_001281492.1:c.-39T=	NP_001268421.1:n.-39T=
NM_001281493.1:c.-775T=	NP_001268422.1:n.-775T=
XM_011532800.1:c.-74T=	XP_011531102.1:n.-74T=
XM_024452819.1:c.-39T=	XP_024308587.1:n.-39T=
XM_024452822.1:c.-775T=	XP_024308590.1:n.-775T=
NM_000179.3:c.-39T= MANE Select	NP_000170.1:n.-39T=
NM_001281492.2:c.-39T=	NP_001268421.1:n.-39T=
NM_001281493.2:c.-775T=	NP_001268422.1:n.-775T=