Canonical Allele Identifier: CA360346812
Gene: MSH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80168949G>A (hg19) chr5:g.80873130G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873130G>A , CM000667.2:g.80873130G>A GRCh38
NC_000005.9:g.80168949G>A , CM000667.1:g.80168949G>A GRCh37
NC_000005.8:g.80204705G>A NCBI36
NG_016607.1:g.223656G>A
NG_016607.2:g.223656G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3145G>A MANE Select ENSP00000265081.6:p.Val1049Ile
ENST00000658259.1:c.2977G>A ENSP00000499617.1:p.Val993Ile
ENST00000659302.1:c.553G>A
ENST00000667069.1:c.2950G>A ENSP00000499502.1:p.Val984Ile
ENST00000670357.1:c.*469G>A ENSP00000499791.1:n.*469G>A
ENST00000265081.6:c.3145G>A ENSP00000265081.6:p.Val1049Ile
NM_002439.4:c.3145G>A NP_002430.3:p.Val1049Ile
NM_002439.5:c.3145G>A MANE Select NP_002430.3:p.Val1049Ile
Search 100 bp 5'
Search 100 bp 3'