Canonical Allele Identifier: CA1558493672

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675118T= , CM000667.2:g.80675118T=	GRCh38
NC_000005.9:g.79970937T= , CM000667.1:g.79970937T=	GRCh37
NC_000005.8:g.80006693T=	NCBI36
NG_016607.1:g.25644T=
NG_016607.2:g.25644T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1163T= MANE Select	ENSP00000265081.6:p.Ile388=
ENST00000658259.1:c.995T=	ENSP00000499617.1:p.Ile332=
ENST00000667069.1:c.1163T=	ENSP00000499502.1:p.Ile388=
ENST00000670357.1:c.1163T=	ENSP00000499791.1:p.Ile388=
ENST00000265081.6:c.1163T=	ENSP00000265081.6:p.Ile388=
NM_002439.4:c.1163T=	NP_002430.3:p.Ile388=
NM_002439.5:c.1163T= MANE Select	NP_002430.3:p.Ile388=