Canonical Allele Identifier: CA1558493041
Gene: MSH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674923A= , CM000667.2:g.80674923A= GRCh38
NC_000005.9:g.79970742A= , CM000667.1:g.79970742A= GRCh37
NC_000005.8:g.80006498A= NCBI36
NG_016607.1:g.25449A=
NG_016607.2:g.25449A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-60A= MANE Select ENSP00000265081.6:n.1028-60A=
ENST00000658259.1:c.860-60A= ENSP00000499617.1:n.860-60A=
ENST00000667069.1:c.1028-60A= ENSP00000499502.1:n.1028-60A=
ENST00000670357.1:c.1028-60A= ENSP00000499791.1:n.1028-60A=
ENST00000265081.6:c.1028-60A= ENSP00000265081.6:n.1028-60A=
NM_002439.4:c.1028-60A= NP_002430.3:n.1028-60A=
NM_002439.5:c.1028-60A= MANE Select NP_002430.3:n.1028-60A=
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