Canonical Allele Identifier: CA360346801

Gene: MSH3

Linked Data

• MyVariant Identifiers: chr5:g.80168944A>T (hg19) ; chr5:g.80873125A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80873125A>T , CM000667.2:g.80873125A>T	GRCh38
NC_000005.9:g.80168944A>T , CM000667.1:g.80168944A>T	GRCh37
NC_000005.8:g.80204700A>T	NCBI36
NG_016607.1:g.223651A>T
NG_016607.2:g.223651A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.3140A>T MANE Select	ENSP00000265081.6:p.Glu1047Val
ENST00000658259.1:c.2972A>T	ENSP00000499617.1:p.Glu991Val
ENST00000659302.1:c.548A>T
ENST00000667069.1:c.2945A>T	ENSP00000499502.1:p.Glu982Val
ENST00000670357.1:c.*464A>T	ENSP00000499791.1:n.*464A>T
ENST00000265081.6:c.3140A>T	ENSP00000265081.6:p.Glu1047Val
NM_002439.4:c.3140A>T	NP_002430.3:p.Glu1047Val
NM_002439.5:c.3140A>T MANE Select	NP_002430.3:p.Glu1047Val