Canonical Allele Identifier: CA1558493992
Gene: MSH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675237A= , CM000667.2:g.80675237A= GRCh38
NC_000005.9:g.79971056A= , CM000667.1:g.79971056A= GRCh37
NC_000005.8:g.80006812A= NCBI36
NG_016607.1:g.25763A=
NG_016607.2:g.25763A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1173+109A= MANE Select ENSP00000265081.6:n.1173+109A=
ENST00000658259.1:c.1005+109A= ENSP00000499617.1:n.1005+109A=
ENST00000667069.1:c.1173+109A= ENSP00000499502.1:n.1173+109A=
ENST00000670357.1:c.1173+109A= ENSP00000499791.1:n.1173+109A=
ENST00000265081.6:c.1173+109A= ENSP00000265081.6:n.1173+109A=
NM_002439.4:c.1173+109A= NP_002430.3:n.1173+109A=
NM_002439.5:c.1173+109A= MANE Select NP_002430.3:n.1173+109A=
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