Canonical Allele Identifier: CA2578350227

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674917A>G , CM000667.2:g.80674917A>G	GRCh38
NC_000005.9:g.79970736A>G , CM000667.1:g.79970736A>G	GRCh37
NC_000005.8:g.80006492A>G	NCBI36
NG_016607.1:g.25443A>G
NG_016607.2:g.25443A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-66A>G MANE Select	ENSP00000265081.6:n.1028-66A>G
ENST00000658259.1:c.860-66A>G	ENSP00000499617.1:n.860-66A>G
ENST00000667069.1:c.1028-66A>G	ENSP00000499502.1:n.1028-66A>G
ENST00000670357.1:c.1028-66A>G	ENSP00000499791.1:n.1028-66A>G
ENST00000265081.6:c.1028-66A>G	ENSP00000265081.6:n.1028-66A>G
NM_002439.4:c.1028-66A>G	NP_002430.3:n.1028-66A>G
NM_002439.5:c.1028-66A>G MANE Select	NP_002430.3:n.1028-66A>G