Canonical Allele Identifier: CA2496037935

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783145A= , CM000664.2:g.47783145A=	GRCh38
NC_000002.11:g.48010284A= , CM000664.1:g.48010284A=	GRCh37
NC_000002.10:g.47863788A=	NCBI36
NG_007111.1:g.4999A= , LRG_219:g.4999A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234420.11:c.-89A= MANE Select	ENSP00000234420.5:n.-89A=
ENST00000652107.1:c.-37-7782A=	ENSP00000498629.1:n.-37-7782A=
ENST00000673922.1:n.1A=
ENST00000234420.9:c.-89A=	ENSP00000234420.4:n.-89A=
ENST00000445503.5:c.-89A=	ENSP00000405294.1:n.-89A=
ENST00000456246.1:c.-89A=	ENSP00000410570.1:n.-89A=
ENST00000540021.5:c.-89A=	ENSP00000446475.1:n.-89A=
ENST00000606499.1:c.-37-7782A=	ENSP00000475605.1:n.-37-7782A=
ENST00000614496.4:c.-825A=	ENSP00000477844.1:n.-825A=
ENST00000622629.4:c.-3185A=	ENSP00000482078.1:n.-3185A=
NM_000179.2:c.-89A= , LRG_219t1:c.-89A=	NP_000170.1:n.-89A=
NM_001281492.1:c.-89A=	NP_001268421.1:n.-89A=
NM_001281493.1:c.-825A=	NP_001268422.1:n.-825A=
XM_024452819.1:c.-89A=	XP_024308587.1:n.-89A=
NM_000179.3:c.-89A= MANE Select	NP_000170.1:n.-89A=
NM_001281492.2:c.-89A=	NP_001268421.1:n.-89A=
NM_001281493.2:c.-825A=	NP_001268422.1:n.-825A=