Canonical Allele Identifier: CA360346797

Gene: MSH3

Linked Data

• MyVariant Identifiers: chr5:g.80168943G>T (hg19) ; chr5:g.80873124G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80873124G>T , CM000667.2:g.80873124G>T	GRCh38
NC_000005.9:g.80168943G>T , CM000667.1:g.80168943G>T	GRCh37
NC_000005.8:g.80204699G>T	NCBI36
NG_016607.1:g.223650G>T
NG_016607.2:g.223650G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265081.7:c.3139G>T MANE Select	ENSP00000265081.6:p.Glu1047Ter
ENST00000658259.1:c.2971G>T	ENSP00000499617.1:p.Glu991Ter
ENST00000659302.1:c.547G>T
ENST00000667069.1:c.2944G>T	ENSP00000499502.1:p.Glu982Ter
ENST00000670357.1:c.*463G>T	ENSP00000499791.1:n.*463G>T
ENST00000265081.6:c.3139G>T	ENSP00000265081.6:p.Glu1047Ter
NM_002439.4:c.3139G>T	NP_002430.3:p.Glu1047Ter
NM_002439.5:c.3139G>T MANE Select	NP_002430.3:p.Glu1047Ter