Canonical Allele Identifier: CA1558493097
Gene: MSH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674973T= , CM000667.2:g.80674973T= GRCh38
NC_000005.9:g.79970792T= , CM000667.1:g.79970792T= GRCh37
NC_000005.8:g.80006548T= NCBI36
NG_016607.1:g.25499T=
NG_016607.2:g.25499T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-10T= MANE Select ENSP00000265081.6:n.1028-10T=
ENST00000658259.1:c.860-10T= ENSP00000499617.1:n.860-10T=
ENST00000667069.1:c.1028-10T= ENSP00000499502.1:n.1028-10T=
ENST00000670357.1:c.1028-10T= ENSP00000499791.1:n.1028-10T=
ENST00000265081.6:c.1028-10T= ENSP00000265081.6:n.1028-10T=
NM_002439.4:c.1028-10T= NP_002430.3:n.1028-10T=
NM_002439.5:c.1028-10T= MANE Select NP_002430.3:n.1028-10T=
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