Canonical Allele Identifier: CA360267939
Gene: MSH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.79970835T>A (hg19) chr5:g.80675016T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675016T>A , CM000667.2:g.80675016T>A GRCh38
NC_000005.9:g.79970835T>A , CM000667.1:g.79970835T>A GRCh37
NC_000005.8:g.80006591T>A NCBI36
NG_016607.1:g.25542T>A
NG_016607.2:g.25542T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1061T>A MANE Select ENSP00000265081.6:p.Val354Glu
ENST00000658259.1:c.893T>A ENSP00000499617.1:p.Val298Glu
ENST00000667069.1:c.1061T>A ENSP00000499502.1:p.Val354Glu
ENST00000670357.1:c.1061T>A ENSP00000499791.1:p.Val354Glu
ENST00000265081.6:c.1061T>A ENSP00000265081.6:p.Val354Glu
NM_002439.4:c.1061T>A NP_002430.3:p.Val354Glu
NM_002439.5:c.1061T>A MANE Select NP_002430.3:p.Val354Glu
Search 100 bp 5'
Search 100 bp 3'