Canonical Allele Identifier: CA2709330050

Gene: MSH3

Linked Data

• dbSNP Id: rs2112816203

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675184_80675185insTTACA , CM000667.2:g.80675184_80675185insTTACA	GRCh38
NC_000005.9:g.79971003_79971004insTTACA , CM000667.1:g.79971003_79971004insTTACA	GRCh37
NC_000005.8:g.80006759_80006760insTTACA	NCBI36
NG_016607.1:g.25710_25711insTTACA
NG_016607.2:g.25710_25711insTTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+56_1173+57insTTACA MANE Select	ENSP00000265081.6:n.1173+56_1173+57insTTACA
ENST00000658259.1:c.1005+56_1005+57insTTACA	ENSP00000499617.1:n.1005+56_1005+57insTTACA
ENST00000667069.1:c.1173+56_1173+57insTTACA	ENSP00000499502.1:n.1173+56_1173+57insTTACA
ENST00000670357.1:c.1173+56_1173+57insTTACA	ENSP00000499791.1:n.1173+56_1173+57insTTACA
ENST00000265081.6:c.1173+56_1173+57insTTACA	ENSP00000265081.6:n.1173+56_1173+57insTTACA
NM_002439.4:c.1173+56_1173+57insTTACA	NP_002430.3:n.1173+56_1173+57insTTACA
NM_002439.5:c.1173+56_1173+57insTTACA MANE Select	NP_002430.3:n.1173+56_1173+57insTTACA