Canonical Allele Identifier: CA1558492942

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674849G= , CM000667.2:g.80674849G=	GRCh38
NC_000005.9:g.79970668G= , CM000667.1:g.79970668G=	GRCh37
NC_000005.8:g.80006424G=	NCBI36
NG_016607.1:g.25375G=
NG_016607.2:g.25375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-134G= MANE Select	ENSP00000265081.6:n.1028-134G=
ENST00000658259.1:c.860-134G=	ENSP00000499617.1:n.860-134G=
ENST00000667069.1:c.1028-134G=	ENSP00000499502.1:n.1028-134G=
ENST00000670357.1:c.1028-134G=	ENSP00000499791.1:n.1028-134G=
ENST00000265081.6:c.1028-134G=	ENSP00000265081.6:n.1028-134G=
NM_002439.4:c.1028-134G=	NP_002430.3:n.1028-134G=
NM_002439.5:c.1028-134G= MANE Select	NP_002430.3:n.1028-134G=