Canonical Allele Identifier: CA1558493022

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674912_80674915delinsATAT , CM000667.2:g.80674912_80674915delinsATAT	GRCh38
NC_000005.9:g.79970731_79970734delinsATAT , CM000667.1:g.79970731_79970734delinsATAT	GRCh37
NC_000005.8:g.80006487_80006490delinsATAT	NCBI36
NG_016607.1:g.25438_25441delinsATAT
NG_016607.2:g.25438_25441delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-71_1028-68delinsATAT MANE Select	ENSP00000265081.6:n.1028-71_1028-68delinsATAT
ENST00000658259.1:c.860-71_860-68delinsATAT	ENSP00000499617.1:n.860-71_860-68delinsATAT
ENST00000667069.1:c.1028-71_1028-68delinsATAT	ENSP00000499502.1:n.1028-71_1028-68delinsATAT
ENST00000670357.1:c.1028-71_1028-68delinsATAT	ENSP00000499791.1:n.1028-71_1028-68delinsATAT
ENST00000265081.6:c.1028-71_1028-68delinsATAT	ENSP00000265081.6:n.1028-71_1028-68delinsATAT
NM_002439.4:c.1028-71_1028-68delinsATAT	NP_002430.3:n.1028-71_1028-68delinsATAT
NM_002439.5:c.1028-71_1028-68delinsATAT MANE Select	NP_002430.3:n.1028-71_1028-68delinsATAT