Canonical Allele Identifier: CA1558493600

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675104G= , CM000667.2:g.80675104G=	GRCh38
NC_000005.9:g.79970923G= , CM000667.1:g.79970923G=	GRCh37
NC_000005.8:g.80006679G=	NCBI36
NG_016607.1:g.25630G=
NG_016607.2:g.25630G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1149G= MANE Select	ENSP00000265081.6:p.Lys383=
ENST00000658259.1:c.981G=	ENSP00000499617.1:p.Lys327=
ENST00000667069.1:c.1149G=	ENSP00000499502.1:p.Lys383=
ENST00000670357.1:c.1149G=	ENSP00000499791.1:p.Lys383=
ENST00000265081.6:c.1149G=	ENSP00000265081.6:p.Lys383=
NM_002439.4:c.1149G=	NP_002430.3:p.Lys383=
NM_002439.5:c.1149G= MANE Select	NP_002430.3:p.Lys383=