Canonical Allele Identifier: CA1558493157

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674987G= , CM000667.2:g.80674987G=	GRCh38
NC_000005.9:g.79970806G= , CM000667.1:g.79970806G=	GRCh37
NC_000005.8:g.80006562G=	NCBI36
NG_016607.1:g.25513G=
NG_016607.2:g.25513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1032G= MANE Select	ENSP00000265081.6:p.Val344=
ENST00000658259.1:c.864G=	ENSP00000499617.1:p.Val288=
ENST00000667069.1:c.1032G=	ENSP00000499502.1:p.Val344=
ENST00000670357.1:c.1032G=	ENSP00000499791.1:p.Val344=
ENST00000265081.6:c.1032G=	ENSP00000265081.6:p.Val344=
NM_002439.4:c.1032G=	NP_002430.3:p.Val344=
NM_002439.5:c.1032G= MANE Select	NP_002430.3:p.Val344=