Canonical Allele Identifier: CA1558516094

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80746456T= , CM000667.2:g.80746456T=	GRCh38
NC_000005.9:g.80042275T= , CM000667.1:g.80042275T=	GRCh37
NC_000005.8:g.80078031T=	NCBI36
NG_016607.1:g.96982T=
NG_016607.2:g.96982T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002439.5:c.1763+1841T= MANE Select	NP_002430.3:n.1763+1841T=
ENST00000265081.7:c.1763+1841T= MANE Select	ENSP00000265081.6:n.1763+1841T=
NM_002439.4:c.1763+1841T=	NP_002430.3:n.1763+1841T=
ENST00000265081.6:c.1763+1841T=	ENSP00000265081.6:n.1763+1841T=
ENST00000506122.1:n.364A=
ENST00000512258.1:n.612+1841T=
ENST00000658259.1:c.1595+1841T=	ENSP00000499617.1:n.1595+1841T=
ENST00000667069.1:c.1569-15090T=	ENSP00000499502.1:n.1569-15090T=
ENST00000670357.1:c.1763+1841T=	ENSP00000499791.1:n.1763+1841T=