Canonical Allele Identifier: CA2709330037

Gene: MSH3

Linked Data

• dbSNP Id: rs2112816199

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675177_80675178insAT , CM000667.2:g.80675177_80675178insAT	GRCh38
NC_000005.9:g.79970996_79970997insAT , CM000667.1:g.79970996_79970997insAT	GRCh37
NC_000005.8:g.80006752_80006753insAT	NCBI36
NG_016607.1:g.25703_25704insAT
NG_016607.2:g.25703_25704insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+49_1173+50insAT MANE Select	ENSP00000265081.6:n.1173+49_1173+50insAT
ENST00000658259.1:c.1005+49_1005+50insAT	ENSP00000499617.1:n.1005+49_1005+50insAT
ENST00000667069.1:c.1173+49_1173+50insAT	ENSP00000499502.1:n.1173+49_1173+50insAT
ENST00000670357.1:c.1173+49_1173+50insAT	ENSP00000499791.1:n.1173+49_1173+50insAT
ENST00000265081.6:c.1173+49_1173+50insAT	ENSP00000265081.6:n.1173+49_1173+50insAT
NM_002439.4:c.1173+49_1173+50insAT	NP_002430.3:n.1173+49_1173+50insAT
NM_002439.5:c.1173+49_1173+50insAT MANE Select	NP_002430.3:n.1173+49_1173+50insAT